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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 2 exons, is associated with 308 variant alleles and maps to 318 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: 2, Coding exons: 0, Transcript length: 592 bps,

Version

ENST00000481254.1

Type

Retained intron

Annotation Method

Manual annotation (determined on a case-by-case basis) from the Havana project.

Alternative transcripts

This transcript corresponds to the following database identifiers:

Havana transcript:
OTTHUMT00000335217 (version 1)

Transcript-based displays