NEW
Try the new Transcript table
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_025161.6 → NP_079437.5 Fanconi anemia core complex-associated protein 100 isoform b
See identical proteins and their annotated locations for NP_079437.5
Status: VALIDATED
- Description
- Transcript Variant: This variant (2) represents the shorter transcript and encodes the functional protein.
- Source sequence(s)
-
AC137896, AL834374, DA103390, DQ989324
- Consensus CDS
-
CCDS32765.2
- UniProtKB/Swiss-Prot
- A6NNM1, Q0VG06, Q8N3F7, Q9BV13, Q9H6K7, Q9H7E8
- UniProtKB/TrEMBL
-
A4ZI32
- Related
- ENSP00000333283.8, ENST00000327787.13
- Conserved Domains (1) summary
-
- pfam15146
Location:449 → 881
- FANCAA; Fanconi anemia-associated
RNA
-
NR_033338.2 RNA Sequence
Status: VALIDATED
- Description
- Transcript Variant: This variant (1) uses an alternate splice site, compared to variant 2. This variant is represented as non-coding because the use of the 5'-most supported translational start codon, as used in variant 2, renders the transcript a candidate for nonsense-mediated mRNA decay (NMD).
- Source sequence(s)
-
AC137896, AL834374, BC008883, DA103390
- Related
-
ENST00000443656.6