Canonical Allele Identifier: CA359827445

Gene: ERCC8

Linked Data

• MyVariant Identifiers: chr5:g.60200692A>T (hg19) ; chr5:g.60904865A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.60904865A>T , CM000667.2:g.60904865A>T	GRCh38
NC_000005.9:g.60200692A>T , CM000667.1:g.60200692A>T	GRCh37
NC_000005.8:g.60236449A>T	NCBI36
NG_009289.1:g.45214T>A , LRG_466:g.45214T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000439176.6:c.408T>A	ENSP00000408344.2:p.Asp136Glu
ENST00000647431.2:c.509T>A	ENSP00000494726.2:n.509T>A
ENST00000647486.2:c.408T>A	ENSP00000494466.2:p.Asp136Glu
ENST00000675042.2:c.234T>A	ENSP00000502082.2:p.Asp78Glu
ENST00000675452.2:c.*373T>A	ENSP00000506954.1:n.*373T>A
ENST00000682217.1:c.408T>A	ENSP00000507570.1:p.Asp136Glu
ENST00000682246.1:n.464T>A
ENST00000682375.1:c.*238T>A	ENSP00000507551.1:n.*238T>A
ENST00000683052.1:c.210T>A	ENSP00000507072.1:p.Asp70Glu
ENST00000683199.1:n.430T>A
ENST00000683216.1:n.673T>A
ENST00000683460.1:c.*238T>A	ENSP00000507820.1:n.*238T>A
ENST00000684394.1:n.463T>A
ENST00000684453.1:n.458T>A
ENST00000684621.1:n.464T>A
ENST00000265038.10:c.408T>A	ENSP00000265038.6:p.Asp136Glu
ENST00000497892.6:c.*206T>A	ENSP00000501805.1:n.*206T>A
ENST00000643034.1:c.*300T>A	ENSP00000496080.1:n.*300T>A
ENST00000643708.1:c.*238T>A	ENSP00000494199.1:n.*238T>A
ENST00000647431.1:c.460T>A
ENST00000647486.1:c.359T>A
ENST00000675042.1:c.234T>A	ENSP00000502082.1:p.Asp78Glu
ENST00000675229.1:c.408T>A	ENSP00000502154.1:p.Asp136Glu
ENST00000675378.1:c.408T>A	ENSP00000502535.1:p.Asp136Glu
ENST00000675452.1:n.657T>A
ENST00000675920.1:n.1016T>A
ENST00000676185.1:c.408T>A MANE Select	ENSP00000501614.1:p.Asp136Glu
ENST00000265038.9:c.408T>A	ENSP00000265038.5:p.Asp136Glu
ENST00000381118.7:c.*452T>A	ENSP00000370510.3:n.*452T>A
ENST00000439176.5:c.234T>A	ENSP00000408344.1:p.Asp78Glu
ENST00000462279.5:n.253T>A
ENST00000484330.5:n.227-2357T>A
ENST00000495985.5:n.181T>A
ENST00000497892.5:n.451T>A
NM_000082.3:c.408T>A , LRG_466t1:c.408T>A	NP_000073.1:p.Asp136Glu
NM_001007233.2:c.234T>A	NP_001007234.1:p.Asp78Glu
NM_001007234.2:c.408T>A	NP_001007235.1:p.Asp136Glu
NM_001290285.1:c.23-1149T>A	NP_001277214.1:n.23-1149T>A
NM_001007234.3:c.408T>A	NP_001007235.1:p.Asp136Glu
NM_000082.4:c.408T>A MANE Select	NP_000073.1:p.Asp136Glu
NM_001007233.3:c.234T>A	NP_001007234.1:p.Asp78Glu
NM_001290285.2:c.23-1149T>A	NP_001277214.1:n.23-1149T>A