Canonical Allele Identifier: CA444468282

Gene: ERCC8

Linked Data

• MyVariant Identifiers: chr5:g.60200620T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.60904793T>G , CM000667.2:g.60904793T>G	GRCh38
NC_000005.9:g.60200620T>G , CM000667.1:g.60200620T>G	GRCh37
NC_000005.8:g.60236377T>G	NCBI36
NG_009289.1:g.45286A>C , LRG_466:g.45286A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000439176.6:c.480A>C	ENSP00000408344.2:p.Ala160=
ENST00000647431.2:c.581A>C	ENSP00000494726.2:n.581A>C
ENST00000647486.2:c.480A>C	ENSP00000494466.2:p.Ala160=
ENST00000675042.2:c.306A>C	ENSP00000502082.2:p.Ala102=
ENST00000675452.2:c.*445A>C	ENSP00000506954.1:n.*445A>C
ENST00000682217.1:c.480A>C	ENSP00000507570.1:p.Ala160=
ENST00000682246.1:n.536A>C
ENST00000682375.1:c.*310A>C	ENSP00000507551.1:n.*310A>C
ENST00000683052.1:c.282A>C	ENSP00000507072.1:p.Ala94=
ENST00000683199.1:n.502A>C
ENST00000683216.1:n.745A>C
ENST00000683460.1:c.*310A>C	ENSP00000507820.1:n.*310A>C
ENST00000684394.1:n.535A>C
ENST00000684453.1:n.530A>C
ENST00000684621.1:n.536A>C
ENST00000265038.10:c.480A>C	ENSP00000265038.6:p.Ala160=
ENST00000497892.6:c.*278A>C	ENSP00000501805.1:n.*278A>C
ENST00000643034.1:c.*372A>C	ENSP00000496080.1:n.*372A>C
ENST00000643708.1:c.*310A>C	ENSP00000494199.1:n.*310A>C
ENST00000647431.1:c.532A>C
ENST00000647486.1:c.431A>C
ENST00000675042.1:c.306A>C	ENSP00000502082.1:p.Ala102=
ENST00000675229.1:c.480A>C	ENSP00000502154.1:p.Ala160=
ENST00000675378.1:c.480A>C	ENSP00000502535.1:p.Ala160=
ENST00000675452.1:n.729A>C
ENST00000675920.1:n.1088A>C
ENST00000676185.1:c.480A>C MANE Select	ENSP00000501614.1:p.Ala160=
ENST00000265038.9:c.480A>C	ENSP00000265038.5:p.Ala160=
ENST00000381118.7:c.*524A>C	ENSP00000370510.3:n.*524A>C
ENST00000439176.5:c.306A>C	ENSP00000408344.1:p.Ala102=
ENST00000462279.5:n.325A>C
ENST00000484330.5:n.227-2285A>C
ENST00000495985.5:n.253A>C
ENST00000497892.5:n.523A>C
NM_000082.3:c.480A>C , LRG_466t1:c.480A>C	NP_000073.1:p.Ala160=
NM_001007233.2:c.306A>C	NP_001007234.1:p.Ala102=
NM_001007234.2:c.480A>C	NP_001007235.1:p.Ala160=
NM_001290285.1:c.23-1077A>C	NP_001277214.1:n.23-1077A>C
NM_001007234.3:c.480A>C	NP_001007235.1:p.Ala160=
NM_000082.4:c.480A>C MANE Select	NP_000073.1:p.Ala160=
NM_001007233.3:c.306A>C	NP_001007234.1:p.Ala102=
NM_001290285.2:c.23-1077A>C	NP_001277214.1:n.23-1077A>C