Canonical Allele Identifier: CA359827232

Gene: ERCC8

Linked Data

• MyVariant Identifiers: chr5:g.60200649G>A (hg19) ; chr5:g.60904822G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.60904822G>A , CM000667.2:g.60904822G>A	GRCh38
NC_000005.9:g.60200649G>A , CM000667.1:g.60200649G>A	GRCh37
NC_000005.8:g.60236406G>A	NCBI36
NG_009289.1:g.45257C>T , LRG_466:g.45257C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000439176.6:c.451C>T	ENSP00000408344.2:p.Pro151Ser
ENST00000647431.2:c.552C>T	ENSP00000494726.2:n.552C>T
ENST00000647486.2:c.451C>T	ENSP00000494466.2:p.Pro151Ser
ENST00000675042.2:c.277C>T	ENSP00000502082.2:p.Pro93Ser
ENST00000675452.2:c.*416C>T	ENSP00000506954.1:n.*416C>T
ENST00000682217.1:c.451C>T	ENSP00000507570.1:p.Pro151Ser
ENST00000682246.1:n.507C>T
ENST00000682375.1:c.*281C>T	ENSP00000507551.1:n.*281C>T
ENST00000683052.1:c.253C>T	ENSP00000507072.1:p.Pro85Ser
ENST00000683199.1:n.473C>T
ENST00000683216.1:n.716C>T
ENST00000683460.1:c.*281C>T	ENSP00000507820.1:n.*281C>T
ENST00000684394.1:n.506C>T
ENST00000684453.1:n.501C>T
ENST00000684621.1:n.507C>T
ENST00000265038.10:c.451C>T	ENSP00000265038.6:p.Pro151Ser
ENST00000497892.6:c.*249C>T	ENSP00000501805.1:n.*249C>T
ENST00000643034.1:c.*343C>T	ENSP00000496080.1:n.*343C>T
ENST00000643708.1:c.*281C>T	ENSP00000494199.1:n.*281C>T
ENST00000647431.1:c.503C>T
ENST00000647486.1:c.402C>T
ENST00000675042.1:c.277C>T	ENSP00000502082.1:p.Pro93Ser
ENST00000675229.1:c.451C>T	ENSP00000502154.1:p.Pro151Ser
ENST00000675378.1:c.451C>T	ENSP00000502535.1:p.Pro151Ser
ENST00000675452.1:n.700C>T
ENST00000675920.1:n.1059C>T
ENST00000676185.1:c.451C>T MANE Select	ENSP00000501614.1:p.Pro151Ser
ENST00000265038.9:c.451C>T	ENSP00000265038.5:p.Pro151Ser
ENST00000381118.7:c.*495C>T	ENSP00000370510.3:n.*495C>T
ENST00000439176.5:c.277C>T	ENSP00000408344.1:p.Pro93Ser
ENST00000462279.5:n.296C>T
ENST00000484330.5:n.227-2314C>T
ENST00000495985.5:n.224C>T
ENST00000497892.5:n.494C>T
NM_000082.3:c.451C>T , LRG_466t1:c.451C>T	NP_000073.1:p.Pro151Ser
NM_001007233.2:c.277C>T	NP_001007234.1:p.Pro93Ser
NM_001007234.2:c.451C>T	NP_001007235.1:p.Pro151Ser
NM_001290285.1:c.23-1106C>T	NP_001277214.1:n.23-1106C>T
NM_001007234.3:c.451C>T	NP_001007235.1:p.Pro151Ser
NM_000082.4:c.451C>T MANE Select	NP_000073.1:p.Pro151Ser
NM_001007233.3:c.277C>T	NP_001007234.1:p.Pro93Ser
NM_001290285.2:c.23-1106C>T	NP_001277214.1:n.23-1106C>T