Canonical Allele Identifier: CA359827353
Gene: ERCC8 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.60904849C>A , CM000667.2:g.60904849C>A GRCh38
NC_000005.9:g.60200676C>A , CM000667.1:g.60200676C>A GRCh37
NC_000005.8:g.60236433C>A NCBI36
NG_009289.1:g.45230G>T , LRG_466:g.45230G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000439176.6:c.424G>T ENSP00000408344.2:p.Glu142Ter
ENST00000647431.2:c.525G>T ENSP00000494726.2:n.525G>T
ENST00000647486.2:c.424G>T ENSP00000494466.2:p.Glu142Ter
ENST00000675042.2:c.250G>T ENSP00000502082.2:p.Glu84Ter
ENST00000675452.2:c.*389G>T ENSP00000506954.1:n.*389G>T
ENST00000682217.1:c.424G>T ENSP00000507570.1:p.Glu142Ter
ENST00000682246.1:n.480G>T
ENST00000682375.1:c.*254G>T ENSP00000507551.1:n.*254G>T
ENST00000683052.1:c.226G>T ENSP00000507072.1:p.Glu76Ter
ENST00000683199.1:n.446G>T
ENST00000683216.1:n.689G>T
ENST00000683460.1:c.*254G>T ENSP00000507820.1:n.*254G>T
ENST00000684394.1:n.479G>T
ENST00000684453.1:n.474G>T
ENST00000684621.1:n.480G>T
ENST00000265038.10:c.424G>T ENSP00000265038.6:p.Glu142Ter
ENST00000497892.6:c.*222G>T ENSP00000501805.1:n.*222G>T
ENST00000643034.1:c.*316G>T ENSP00000496080.1:n.*316G>T
ENST00000643708.1:c.*254G>T ENSP00000494199.1:n.*254G>T
ENST00000647431.1:c.476G>T
ENST00000647486.1:c.375G>T
ENST00000675042.1:c.250G>T ENSP00000502082.1:p.Glu84Ter
ENST00000675229.1:c.424G>T ENSP00000502154.1:p.Glu142Ter
ENST00000675378.1:c.424G>T ENSP00000502535.1:p.Glu142Ter
ENST00000675452.1:n.673G>T
ENST00000675920.1:n.1032G>T
ENST00000676185.1:c.424G>T MANE Select ENSP00000501614.1:p.Glu142Ter
ENST00000265038.9:c.424G>T ENSP00000265038.5:p.Glu142Ter
ENST00000381118.7:c.*468G>T ENSP00000370510.3:n.*468G>T
ENST00000439176.5:c.250G>T ENSP00000408344.1:p.Glu84Ter
ENST00000462279.5:n.269G>T
ENST00000484330.5:n.227-2341G>T
ENST00000495985.5:n.197G>T
ENST00000497892.5:n.467G>T
NM_000082.3:c.424G>T , LRG_466t1:c.424G>T NP_000073.1:p.Glu142Ter
NM_001007233.2:c.250G>T NP_001007234.1:p.Glu84Ter
NM_001007234.2:c.424G>T NP_001007235.1:p.Glu142Ter
NM_001290285.1:c.23-1133G>T NP_001277214.1:n.23-1133G>T
NM_001007234.3:c.424G>T NP_001007235.1:p.Glu142Ter
NM_000082.4:c.424G>T MANE Select NP_000073.1:p.Glu142Ter
NM_001007233.3:c.250G>T NP_001007234.1:p.Glu84Ter
NM_001290285.2:c.23-1133G>T NP_001277214.1:n.23-1133G>T