Canonical Allele Identifier: CA359822276

Gene: ERCC8

Linked Data

• MyVariant Identifiers: chr5:g.60183268T>G (hg19) ; chr5:g.60887441T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.60887441T>G , CM000667.2:g.60887441T>G	GRCh38
NC_000005.9:g.60183268T>G , CM000667.1:g.60183268T>G	GRCh37
NC_000005.8:g.60219025T>G	NCBI36
NG_009289.1:g.62638A>C , LRG_466:g.62638A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000439176.6:c.855+10835A>C	ENSP00000408344.2:n.855+10835A>C
ENST00000647431.2:c.1222A>C	ENSP00000494726.2:n.1222A>C
ENST00000675042.2:c.947A>C	ENSP00000502082.2:p.Glu316Ala
ENST00000675452.2:c.*1086A>C	ENSP00000506954.1:n.*1086A>C
ENST00000682217.1:c.923A>C	ENSP00000507570.1:p.Glu308Ala
ENST00000682375.1:c.*951A>C	ENSP00000507551.1:n.*951A>C
ENST00000683052.1:c.923A>C	ENSP00000507072.1:p.Glu308Ala
ENST00000683216.1:n.4758A>C
ENST00000683460.1:c.*2558A>C	ENSP00000507820.1:n.*2558A>C
ENST00000683688.1:n.2867A>C
ENST00000684621.1:n.979A>C
ENST00000265038.10:c.1178A>C	ENSP00000265038.6:p.Glu393Ala
ENST00000643034.1:c.*1013A>C	ENSP00000496080.1:n.*1013A>C
ENST00000643708.1:c.*951A>C	ENSP00000494199.1:n.*951A>C
ENST00000647431.1:c.1173A>C
ENST00000675378.1:c.*122A>C	ENSP00000502535.1:n.*122A>C
ENST00000675452.1:n.1370A>C
ENST00000676185.1:c.1121A>C MANE Select	ENSP00000501614.1:p.Glu374Ala
ENST00000265038.9:c.1121A>C	ENSP00000265038.5:p.Glu374Ala
ENST00000381118.7:c.*1165A>C	ENSP00000370510.3:n.*1165A>C
ENST00000462279.5:n.2573A>C
NM_000082.3:c.1121A>C , LRG_466t1:c.1121A>C	NP_000073.1:p.Glu374Ala
NM_001007233.2:c.947A>C	NP_001007234.1:p.Glu316Ala
NM_001290285.1:c.662A>C	NP_001277214.1:p.Glu221Ala
NM_000082.4:c.1121A>C MANE Select	NP_000073.1:p.Glu374Ala
NM_001007233.3:c.947A>C	NP_001007234.1:p.Glu316Ala
NM_001290285.2:c.662A>C	NP_001277214.1:p.Glu221Ala