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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_001162980.2 → NP_001156452.2 FYN-binding protein 2 isoform b
Status: VALIDATED
- Description
- Transcript Variant: This variant (2) lacks an alternate in-frame exon in the central coding region, compared to variant 1, resulting in an isoform (b) that is shorter than isoform a.
- Source sequence(s)
-
AL627186, AL929466
- Consensus CDS
-
CCDS51250.2
- UniProtKB/Swiss-Prot
-
A2A995
- UniProtKB/TrEMBL
-
B2RQ28
- Related
- ENSMUSP00000102416.2, ENSMUST00000106804.2
- Conserved Domains (1) summary
-
- cl17036
Location:651 → 723
- SH3; Src Homology 3 domain superfamily
-
NM_001285952.2 → NP_001272881.2 FYN-binding protein 2 isoform a
Status: VALIDATED
- Description
- Transcript Variant: This variant (1) represents the longest transcript and encodes the longest isoform (a).
- Source sequence(s)
-
AL627186, AL929466
- UniProtKB/TrEMBL
-
B2RQ28
- Conserved Domains (1) summary
-
- cl17036
Location:677 → 749
- SH3; Src Homology 3 domain superfamily
-
NM_001285953.2 → NP_001272882.1 FYN-binding protein 2 isoform c
See identical proteins and their annotated locations for NP_001272882.1
Status: VALIDATED
- Description
- Transcript Variant: This variant (3) differs in its 5' UTR, initiates translation at a downstream in-frame start codon, and lacks an alternate in-frame exon in the central coding region, compared to variant 1. The encoded isoform (c) is shorter at the N-terminus, compared to isoform a.
- Source sequence(s)
-
AL627186, AL929466
- UniProtKB/TrEMBL
-
B2RQ28
- Conserved Domains (1) summary
-
- cl17036
Location:624 → 696
- SH3; Src Homology 3 domain superfamily
RNA
-
NR_104376.2 RNA Sequence
Status: VALIDATED
- Description
- Transcript Variant: This variant (4) lacks an alternate exon and uses an alternate splice site in the central region, and includes an additional exon in the 3' region, compared to variant 1. This variant is represented as non-coding because use of the 5'-most expected translational start codon, as used in variant 1, renders the transcript a candidate for nonsense-mediated mRNA decay (NMD).
- Source sequence(s)
-
AL627186, AL929466