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These reference sequences exist independently of genome builds. Explain
These reference sequences are curated independently of the genome
annotation cycle, so their versions may not match the RefSeq versions in the current
genome build. Identify version mismatches by comparing the version of the RefSeq in
this section to the one reported in Genomic regions,
transcripts, and products above.
mRNA and Protein(s)
-
NM_001178100.2 → NP_001171571.1 T-cell surface glycoprotein CD8 beta chain isoform 6 precursor
See identical proteins and their annotated locations for NP_001171571.1
Status: REVIEWED
- Description
- Transcript Variant: This variant (6) lacks two exons in the 3' coding region, which results in a frameshift, compared to variant 2. The resulting protein (isoform 6) is shorter and has a distinct C-terminus compared to isoform 2.
- Source sequence(s)
-
AW296309, BC100912, DC405359, X13445
- Consensus CDS
-
CCDS54376.1
- UniProtKB/TrEMBL
-
Q9UQ56
- Related
- ENSP00000377358.2, ENST00000393761.6
- Conserved Domains (2) summary
-
- cd07700
Location:29 → 134
- IgV_CD8_beta; Immunoglobulin (Ig) like domain of CD8 beta chain
- smart00410
Location:26 → 134
- IG_like; Immunoglobulin like
-
NM_004931.5 → NP_004922.1 T-cell surface glycoprotein CD8 beta chain isoform 5 precursor
See identical proteins and their annotated locations for NP_004922.1
Status: REVIEWED
- Description
- Transcript Variant: This variant (5), also known as M-1, differs in the 3' coding region and 3' UTR, compared to variant 1. The resulting isoform (2) has a distinct C-terminus and is shorter than isoform 2.
- Source sequence(s)
-
AC111200, BC100912, BP392114, DB223179, DC405359, X13444
- Consensus CDS
-
CCDS1997.1
- UniProtKB/Swiss-Prot
- P10966, P14860, P14861, Q15980, Q496E0, Q496E1, Q496E2, Q9UDB4, Q9UDB5, Q9UDB6, Q9UDB7, Q9UDB8, Q9UDB9, Q9UDC0, Q9UQ55
- UniProtKB/TrEMBL
-
E9PD41
- Related
- ENSP00000375070.6, ENST00000390655.12
- Conserved Domains (2) summary
-
- cd07700
Location:29 → 134
- IgV_CD8_beta; Immunoglobulin (Ig) like domain of CD8 beta chain
- smart00410
Location:26 → 134
- IG_like; Immunoglobulin like
-
NM_172101.5 → NP_742099.1 T-cell surface glycoprotein CD8 beta chain isoform 3 precursor
See identical proteins and their annotated locations for NP_742099.1
Status: REVIEWED
- Description
- Transcript Variant: This variant (3), also known as M-3, includes an alternate exon in the 3' coding region, which results in a frameshift compared to variant 2. The resulting membrane associated protein (isoform 3) is shorter and has a distinct C-terminus, compared to isoform 2.
- Source sequence(s)
-
AW296309, BC100912, DC405359, X13445
- Consensus CDS
-
CCDS42708.1
- UniProtKB/TrEMBL
- B4E0F8, E7EPH5
- Related
- ENSP00000377356.2, ENST00000393759.6
- Conserved Domains (2) summary
-
- cd07700
Location:29 → 134
- IgV_CD8_beta; Immunoglobulin (Ig) like domain of CD8 beta chain
- smart00410
Location:26 → 134
- IG_like; Immunoglobulin like
-
NM_172102.5 → NP_742100.1 T-cell surface glycoprotein CD8 beta chain isoform 4 precursor
See identical proteins and their annotated locations for NP_742100.1
Status: REVIEWED
- Description
- Transcript Variant: This variant (4), also known as S-1, lacks an in-frame exon in the coding region, compared to variant 2. The resulting secreted protein (isoform 4) is shorter than isoform 2.
- Source sequence(s)
-
AW296309, BC100912, DC405359, X13446
- Consensus CDS
-
CCDS1994.1
- UniProtKB/TrEMBL
- B4E0F8, E7EPH5
- Related
- ENSP00000340592.3, ENST00000349455.7
- Conserved Domains (2) summary
-
- cd07700
Location:29 → 134
- IgV_CD8_beta; Immunoglobulin (Ig) like domain of CD8 beta chain
- smart00410
Location:26 → 134
- IG_like; Immunoglobulin like
-
NM_172213.5 → NP_757362.1 T-cell surface glycoprotein CD8 beta chain isoform 2 precursor
See identical proteins and their annotated locations for NP_757362.1
Status: REVIEWED
- Description
- Transcript Variant: This variant (2) encodes the longest isoform (2).
- Source sequence(s)
-
AW296309, BC100912, BC100913, DC405359
- Consensus CDS
-
CCDS1995.1
- UniProtKB/TrEMBL
- B4E0F8, E7EPH5
- Related
- ENSP00000331172.2, ENST00000331469.6
- Conserved Domains (1) summary
-
- cd07700
Location:29 → 134
- IgV_CD8_beta; Immunoglobulin (Ig) like domain of CD8 beta chain
The following sections contain reference sequences that belong to a
specific genome build. Explain
This section includes genomic Reference
Sequences (RefSeqs) from all assemblies on which this gene is annotated, such as
RefSeqs for chromosomes and scaffolds (contigs) from both reference and alternate
assemblies. Model RNAs and proteins are also reported here.
Reference GRCh38.p14 Primary Assembly
Genomic
-
NC_000002.12 Reference GRCh38.p14 Primary Assembly
- Range
-
86815369..86861886 complement
- Download
- GenBank, FASTA, Sequence Viewer (Graphics)
mRNA and Protein(s)
-
XM_011533164.3 → XP_011531466.1 T-cell surface glycoprotein CD8 beta chain isoform X1
See identical proteins and their annotated locations for XP_011531466.1
- UniProtKB/TrEMBL
- B4E0F8, E7EPH5, E9PD41, Q53QL8
- Conserved Domains (2) summary
-
- cd07700
Location:29 → 134
- IgV_CD8_beta; Immunoglobulin (Ig) like domain of CD8 beta chain
- smart00410
Location:26 → 134
- IG_like; Immunoglobulin like
Alternate T2T-CHM13v2.0
Genomic
-
NC_060926.1 Alternate T2T-CHM13v2.0
- Range
-
86817280..86863804 complement
- Download
- GenBank, FASTA, Sequence Viewer (Graphics)
mRNA and Protein(s)
-
XM_054344557.1 → XP_054200532.1 T-cell surface glycoprotein CD8 beta chain isoform X1
- UniProtKB/TrEMBL
- B4E0F8, E7EPH5, E9PD41, Q53QL8
The following Reference Sequences have been suppressed. Explain
These RefSeqs were suppressed for the
cited reason(s). Suppressed RefSeqs do not appear in BLAST databases, related
sequence links, or BLAST links (BLink), but may still be retrieved by clicking on
their accession.version below.
-
NM_172099.2: Suppressed sequence
- Description
- NM_172099.2: This RefSeq was temporarily suppressed because currently there is not sufficient data to support this transcript.
-
NM_172100.1: Suppressed sequence
- Description
- NM_172100.1: This RefSeq record was removed by NCBI staff. Contact [email protected] for further information.