Human (GRCh37.p13)
Description

excision repair cross-complementing rodent repair deficiency, complementation group 5 [Source:HGNC Symbol;Acc:3437]

Gene Synonyms

COFS3, ERCM2, UVDR, XPG, XPGC

Location

Chromosome 13: 103,497,194-103,528,345 forward strand.

GRCh37:CM000675.1

About this gene

This gene has 7 transcripts (splice variants), 1 paralogue and is associated with 73 phenotypes.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeqFlags
ENST00000355739.4ERCC5-00150761186aaENSP00000347978.4
 
Protein coding
CCDS32004P28715 NM_000123.3GENCODE basic
ENST00000375954.1ERCC5-0062986419aaENSP00000365121.1
 
Protein coding
P28715 -GENCODE basic
ENST00000535557.1ERCC5-2011142232aaENSP00000442117.1
 
Protein coding
Q9HD60 -GENCODE basic
ENST00000472151.1ERCC5-00263543aaENSP00000436083.1
 
Nonsense mediated decay
F2Z2A1 --
ENST00000472247.1ERCC5-005710No protein-
 
Processed transcript
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ENST00000481099.1ERCC5-004798No protein-
 
Retained intron
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ENST00000375958.3ERCC5-003596No protein-
 
Retained intron
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