Human (GRCh37.p13)
Description

excision repair cross-complementing rodent repair deficiency, complementation group 2 [Source:HGNC Symbol;Acc:3434]

Gene Synonyms

COFS2, EM9, MAG, MGC102762, MGC126218, MGC126219, TTD, XPD, XPDC

Location

Chromosome 19: 45,853,095-45,874,176 reverse strand.

GRCh37:CM000681.1

About this gene

This gene has 14 transcripts (splice variants) and is associated with 74 phenotypes.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeqFlags
ENST00000391945.4ERCC2-0014153760aaENSP00000375809.3
 
Protein coding
CCDS33049A8MX75 K7EIT8 P18074
NM_000400.3GENCODE basic
ENST00000391941.2ERCC2-0052871706aaENSP00000375805.2
 
Protein coding
A8MX75 K7EIT8 -CDS 3' incomplete
ENST00000391944.3ERCC2-2032103682aaENSP00000375808.3
 
Protein coding
E7EVE9 -GENCODE basic
ENST00000485403.2ERCC2-0061538405aaENSP00000431229.2
 
Protein coding
CCDS46112K7EIT8 P18074 NM_001130867.1GENCODE basic
ENST00000391940.4ERCC2-2021300405aaENSP00000375804.4
 
Protein coding
CCDS46112K7EIT8 P18074 -GENCODE basic
ENST00000586131.1ERCC2-0021007292aaENSP00000464887.1
 
Protein coding
K7EIT8 -CDS 3' incomplete
ENST00000221481.6ERCC2-201745127aaENSP00000221481.6
 
Protein coding
B4E0F6 -GENCODE basic
ENST00000586856.1ERCC2-003690109aaENSP00000466998.1
 
Protein coding
K7ENL1 -CDS 3' incomplete
ENST00000587376.1ERCC2-004817202aaENSP00000465593.1
 
Nonsense mediated decay
--CDS 5' incomplete
ENST00000591309.1ERCC2-011557127aaENSP00000465207.1
 
Nonsense mediated decay
B4E0F6 --
ENST00000588652.1ERCC2-0082405No protein-
 
Retained intron
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ENST00000391942.2ERCC2-0071488No protein-
 
Retained intron
---
ENST00000586441.1ERCC2-010682No protein-
 
Retained intron
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ENST00000586737.1ERCC2-009481No protein-
 
Retained intron
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