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Human (GRCh37.p13)
Description

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

Gene Synonyms

FAG, XRCC9

Location
About this transcript

This transcript has 14 exons, is annotated with 18 domains and features, is associated with 2391 variant alleles and maps to 602 oligo probes.

Gene
NameTranscript IDbpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeqFlags
FANCG-001ENST00000378643.32631622aaENSP00000367910.3
 
Protein coding
CCDS6574C9JSE3 O15287 Q53XM5
NM_004629
NP_004620
GENCODE basic
FANCG-003ENST00000448890.1868215aaENSP00000409607.1
 
Protein coding
-C9JSE3 -CDS 3' incomplete
FANCG-005ENST00000425676.12108106aaENSP00000412793.1
 
Nonsense mediated decay
-F8WC08 --
FANCG-002ENST00000476212.1484No protein-
 
Processed transcript
----
FANCG-004ENST00000462124.1654No protein-
 
Retained intron
----
FANCG-008ENST00000481254.1592No protein-
 
Retained intron
----
FANCG-006ENST00000474894.1572No protein-
 
Retained intron
----
FANCG-007ENST00000461149.1388No protein-
 
Retained intron
----
Statistics

Exons: 14, Coding exons: 14, Transcript length: 2,631 bps, Translation length: 622 residues

CCDS

This transcript is a member of the Human CCDS set: CCDS6574

Uniprot

This transcript corresponds to the following Uniprot identifiers: O15287

Version

ENST00000378643.3

Type

Protein coding

Annotation Method

Transcript where the Ensembl genebuild transcript and the Havana manual annotation have the same sequence, for every base pair. See article.

Alternative transcripts

This transcript corresponds to the following database identifiers:

Transcript having exact match between ENSEMBL and HAVANA:
OTTHUMT00000052269 (version 1)
GENCODE basic gene

This transcript is a member of the Gencode basic gene set.

Transcript-based displays