Human (GRCh37.p13)
Description

Fanconi anemia, complementation group G [Source:HGNC Symbol;Acc:3588]

Gene Synonyms

FAG, XRCC9

Location

Chromosome 9: 35,073,832-35,080,013 reverse strand.

GRCh37:CM000671.1

About this gene

This gene has 8 transcripts (splice variants) and is associated with 48 phenotypes.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeqFlags
ENST00000378643.3FANCG-0012631622aaENSP00000367910.3
 
Protein coding
CCDS6574C9JSE3 O15287 Q53XM5
NM_004629.1GENCODE basic
ENST00000448890.1FANCG-003868215aaENSP00000409607.1
 
Protein coding
C9JSE3 -CDS 3' incomplete
ENST00000425676.1FANCG-0052108106aaENSP00000412793.1
 
Nonsense mediated decay
F8WC08 --
ENST00000476212.1FANCG-002484No protein-
 
Processed transcript
---
ENST00000462124.1FANCG-004654No protein-
 
Retained intron
---
ENST00000481254.1FANCG-008592No protein-
 
Retained intron
---
ENST00000474894.1FANCG-006572No protein-
 
Retained intron
---
ENST00000461149.1FANCG-007388No protein-
 
Retained intron
---