Canonical Allele Identifier: CA1549989110
Gene: ERCC8 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.60904823A= , CM000667.2:g.60904823A= GRCh38
NC_000005.9:g.60200650A= , CM000667.1:g.60200650A= GRCh37
NC_000005.8:g.60236407A= NCBI36
NG_009289.1:g.45256T= , LRG_466:g.45256T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000439176.6:c.450T= ENSP00000408344.2:p.Ser150=
ENST00000647431.2:c.551T= ENSP00000494726.2:n.551T=
ENST00000647486.2:c.450T= ENSP00000494466.2:p.Ser150=
ENST00000675042.2:c.276T= ENSP00000502082.2:p.Ser92=
ENST00000675452.2:c.*415T= ENSP00000506954.1:n.*415T=
ENST00000682217.1:c.450T= ENSP00000507570.1:p.Ser150=
ENST00000682246.1:n.506T=
ENST00000682375.1:c.*280T= ENSP00000507551.1:n.*280T=
ENST00000683052.1:c.252T= ENSP00000507072.1:p.Ser84=
ENST00000683199.1:n.472T=
ENST00000683216.1:n.715T=
ENST00000683460.1:c.*280T= ENSP00000507820.1:n.*280T=
ENST00000684394.1:n.505T=
ENST00000684453.1:n.500T=
ENST00000684621.1:n.506T=
ENST00000265038.10:c.450T= ENSP00000265038.6:p.Ser150=
ENST00000497892.6:c.*248T= ENSP00000501805.1:n.*248T=
ENST00000643034.1:c.*342T= ENSP00000496080.1:n.*342T=
ENST00000643708.1:c.*280T= ENSP00000494199.1:n.*280T=
ENST00000647431.1:c.502T=
ENST00000647486.1:c.401T=
ENST00000675042.1:c.276T= ENSP00000502082.1:p.Ser92=
ENST00000675229.1:c.450T= ENSP00000502154.1:p.Ser150=
ENST00000675378.1:c.450T= ENSP00000502535.1:p.Ser150=
ENST00000675452.1:n.699T=
ENST00000675920.1:n.1058T=
ENST00000676185.1:c.450T= MANE Select ENSP00000501614.1:p.Ser150=
ENST00000265038.9:c.450T= ENSP00000265038.5:p.Ser150=
ENST00000381118.7:c.*494T= ENSP00000370510.3:n.*494T=
ENST00000439176.5:c.276T= ENSP00000408344.1:p.Ser92=
ENST00000462279.5:n.295T=
ENST00000484330.5:n.227-2315T=
ENST00000495985.5:n.223T=
ENST00000497892.5:n.493T=
NM_000082.3:c.450T= , LRG_466t1:c.450T= NP_000073.1:p.Ser150=
NM_001007233.2:c.276T= NP_001007234.1:p.Ser92=
NM_001007234.2:c.450T= NP_001007235.1:p.Ser150=
NM_001290285.1:c.23-1107T= NP_001277214.1:n.23-1107T=
NM_001007234.3:c.450T= NP_001007235.1:p.Ser150=
NM_000082.4:c.450T= MANE Select NP_000073.1:p.Ser150=
NM_001007233.3:c.276T= NP_001007234.1:p.Ser92=
NM_001290285.2:c.23-1107T= NP_001277214.1:n.23-1107T=