Canonical Allele Identifier: CA1549983001

Gene: ERCC8

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.60890964G= , CM000667.2:g.60890964G=	GRCh38
NC_000005.9:g.60186791G= , CM000667.1:g.60186791G=	GRCh37
NC_000005.8:g.60222548G=	NCBI36
NG_009289.1:g.59115C= , LRG_466:g.59115C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000439176.6:c.855+7312C=	ENSP00000408344.2:n.855+7312C=
ENST00000647431.2:c.1067C=	ENSP00000494726.2:n.1067C=
ENST00000647486.2:c.1237C=	ENSP00000494466.2:n.1237C=
ENST00000675042.2:c.792C=	ENSP00000502082.2:p.Tyr264=
ENST00000675452.2:c.*931C=	ENSP00000506954.1:n.*931C=
ENST00000682217.1:c.844-3444C=	ENSP00000507570.1:n.844-3444C=
ENST00000682375.1:c.*796C=	ENSP00000507551.1:n.*796C=
ENST00000683052.1:c.768C=	ENSP00000507072.1:p.Tyr256=
ENST00000683199.1:n.988C=
ENST00000683216.1:n.1235C=
ENST00000683460.1:c.*2403C=	ENSP00000507820.1:n.*2403C=
ENST00000684453.1:n.2623C=
ENST00000684621.1:n.900-3444C=
ENST00000265038.10:c.1023C=	ENSP00000265038.6:p.Tyr341=
ENST00000643034.1:c.*858C=	ENSP00000496080.1:n.*858C=
ENST00000643708.1:c.*796C=	ENSP00000494199.1:n.*796C=
ENST00000647431.1:c.1018C=
ENST00000647486.1:c.1188C=
ENST00000675378.1:c.966C=	ENSP00000502535.1:p.Tyr322=
ENST00000675452.1:n.1215C=
ENST00000676185.1:c.966C= MANE Select	ENSP00000501614.1:p.Tyr322=
ENST00000265038.9:c.966C=	ENSP00000265038.5:p.Tyr322=
ENST00000381118.7:c.*1010C=	ENSP00000370510.3:n.*1010C=
ENST00000462279.5:n.2418C=
NM_000082.3:c.966C= , LRG_466t1:c.966C=	NP_000073.1:p.Tyr322=
NM_001007233.2:c.792C=	NP_001007234.1:p.Tyr264=
NM_001290285.1:c.507C=	NP_001277214.1:p.Tyr169=
NM_000082.4:c.966C= MANE Select	NP_000073.1:p.Tyr322=
NM_001007233.3:c.792C=	NP_001007234.1:p.Tyr264=
NM_001290285.2:c.507C=	NP_001277214.1:p.Tyr169=