Canonical Allele Identifier: CA118853700

Gene: ERCC8

Linked Data

• dbSNP Id: rs895140713
• gnomAD v3: 5-60904862-T-A
• gnomAD v4: 5-60904862-T-A
• MyVariant Identifiers: chr5:g.60200689T>A (hg19) ; chr5:g.60904862T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.60904862T>A , CM000667.2:g.60904862T>A	GRCh38
NC_000005.9:g.60200689T>A , CM000667.1:g.60200689T>A	GRCh37
NC_000005.8:g.60236446T>A	NCBI36
NG_009289.1:g.45217A>T , LRG_466:g.45217A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000439176.6:c.411A>T	ENSP00000408344.2:p.Val137=
ENST00000647431.2:c.512A>T	ENSP00000494726.2:n.512A>T
ENST00000647486.2:c.411A>T	ENSP00000494466.2:p.Val137=
ENST00000675042.2:c.237A>T	ENSP00000502082.2:p.Val79=
ENST00000675452.2:c.*376A>T	ENSP00000506954.1:n.*376A>T
ENST00000682217.1:c.411A>T	ENSP00000507570.1:p.Val137=
ENST00000682246.1:n.467A>T
ENST00000682375.1:c.*241A>T	ENSP00000507551.1:n.*241A>T
ENST00000683052.1:c.213A>T	ENSP00000507072.1:p.Val71=
ENST00000683199.1:n.433A>T
ENST00000683216.1:n.676A>T
ENST00000683460.1:c.*241A>T	ENSP00000507820.1:n.*241A>T
ENST00000684394.1:n.466A>T
ENST00000684453.1:n.461A>T
ENST00000684621.1:n.467A>T
ENST00000265038.10:c.411A>T	ENSP00000265038.6:p.Val137=
ENST00000497892.6:c.*209A>T	ENSP00000501805.1:n.*209A>T
ENST00000643034.1:c.*303A>T	ENSP00000496080.1:n.*303A>T
ENST00000643708.1:c.*241A>T	ENSP00000494199.1:n.*241A>T
ENST00000647431.1:c.463A>T
ENST00000647486.1:c.362A>T
ENST00000675042.1:c.237A>T	ENSP00000502082.1:p.Val79=
ENST00000675229.1:c.411A>T	ENSP00000502154.1:p.Val137=
ENST00000675378.1:c.411A>T	ENSP00000502535.1:p.Val137=
ENST00000675452.1:n.660A>T
ENST00000675920.1:n.1019A>T
ENST00000676185.1:c.411A>T MANE Select	ENSP00000501614.1:p.Val137=
ENST00000265038.9:c.411A>T	ENSP00000265038.5:p.Val137=
ENST00000381118.7:c.*455A>T	ENSP00000370510.3:n.*455A>T
ENST00000439176.5:c.237A>T	ENSP00000408344.1:p.Val79=
ENST00000462279.5:n.256A>T
ENST00000484330.5:n.227-2354A>T
ENST00000495985.5:n.184A>T
ENST00000497892.5:n.454A>T
NM_000082.3:c.411A>T , LRG_466t1:c.411A>T	NP_000073.1:p.Val137=
NM_001007233.2:c.237A>T	NP_001007234.1:p.Val79=
NM_001007234.2:c.411A>T	NP_001007235.1:p.Val137=
NM_001290285.1:c.23-1146A>T	NP_001277214.1:n.23-1146A>T
NM_001007234.3:c.411A>T	NP_001007235.1:p.Val137=
NM_000082.4:c.411A>T MANE Select	NP_000073.1:p.Val137=
NM_001007233.3:c.237A>T	NP_001007234.1:p.Val79=
NM_001290285.2:c.23-1146A>T	NP_001277214.1:n.23-1146A>T