Canonical Allele Identifier: CA359827277

Gene: ERCC8

Linked Data

• dbSNP Id: rs1318548083
• gnomAD v3: 5-60904830-T-C
• gnomAD v4: 5-60904830-T-C
• MyVariant Identifiers: chr5:g.60200657T>C (hg19) ; chr5:g.60904830T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.60904830T>C , CM000667.2:g.60904830T>C	GRCh38
NC_000005.9:g.60200657T>C , CM000667.1:g.60200657T>C	GRCh37
NC_000005.8:g.60236414T>C	NCBI36
NG_009289.1:g.45249A>G , LRG_466:g.45249A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000439176.6:c.443A>G	ENSP00000408344.2:p.His148Arg
ENST00000647431.2:c.544A>G	ENSP00000494726.2:n.544A>G
ENST00000647486.2:c.443A>G	ENSP00000494466.2:p.His148Arg
ENST00000675042.2:c.269A>G	ENSP00000502082.2:p.His90Arg
ENST00000675452.2:c.*408A>G	ENSP00000506954.1:n.*408A>G
ENST00000682217.1:c.443A>G	ENSP00000507570.1:p.His148Arg
ENST00000682246.1:n.499A>G
ENST00000682375.1:c.*273A>G	ENSP00000507551.1:n.*273A>G
ENST00000683052.1:c.245A>G	ENSP00000507072.1:p.His82Arg
ENST00000683199.1:n.465A>G
ENST00000683216.1:n.708A>G
ENST00000683460.1:c.*273A>G	ENSP00000507820.1:n.*273A>G
ENST00000684394.1:n.498A>G
ENST00000684453.1:n.493A>G
ENST00000684621.1:n.499A>G
ENST00000265038.10:c.443A>G	ENSP00000265038.6:p.His148Arg
ENST00000497892.6:c.*241A>G	ENSP00000501805.1:n.*241A>G
ENST00000643034.1:c.*335A>G	ENSP00000496080.1:n.*335A>G
ENST00000643708.1:c.*273A>G	ENSP00000494199.1:n.*273A>G
ENST00000647431.1:c.495A>G
ENST00000647486.1:c.394A>G
ENST00000675042.1:c.269A>G	ENSP00000502082.1:p.His90Arg
ENST00000675229.1:c.443A>G	ENSP00000502154.1:p.His148Arg
ENST00000675378.1:c.443A>G	ENSP00000502535.1:p.His148Arg
ENST00000675452.1:n.692A>G
ENST00000675920.1:n.1051A>G
ENST00000676185.1:c.443A>G MANE Select	ENSP00000501614.1:p.His148Arg
ENST00000265038.9:c.443A>G	ENSP00000265038.5:p.His148Arg
ENST00000381118.7:c.*487A>G	ENSP00000370510.3:n.*487A>G
ENST00000439176.5:c.269A>G	ENSP00000408344.1:p.His90Arg
ENST00000462279.5:n.288A>G
ENST00000484330.5:n.227-2322A>G
ENST00000495985.5:n.216A>G
ENST00000497892.5:n.486A>G
NM_000082.3:c.443A>G , LRG_466t1:c.443A>G	NP_000073.1:p.His148Arg
NM_001007233.2:c.269A>G	NP_001007234.1:p.His90Arg
NM_001007234.2:c.443A>G	NP_001007235.1:p.His148Arg
NM_001290285.1:c.23-1114A>G	NP_001277214.1:n.23-1114A>G
NM_001007234.3:c.443A>G	NP_001007235.1:p.His148Arg
NM_000082.4:c.443A>G MANE Select	NP_000073.1:p.His148Arg
NM_001007233.3:c.269A>G	NP_001007234.1:p.His90Arg
NM_001290285.2:c.23-1114A>G	NP_001277214.1:n.23-1114A>G