Canonical Allele Identifier: CA406203394
Gene: XRCC1 HGNC NCBI

Linked Data

dbSNP Id: rs2146048984

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.43551622T>A , CM000681.2:g.43551622T>A GRCh38
NC_000019.9:g.44055774T>A , CM000681.1:g.44055774T>A GRCh37
NC_000019.8:g.48747614T>A NCBI36
NG_033799.1:g.28957A>T , LRG_784:g.28957A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000262887.10:c.1148A>T MANE Select ENSP00000262887.5:p.Lys383Met
ENST00000262887.9:c.1148A>T ENSP00000262887.4:p.Lys383Met
ENST00000543982.5:c.1055A>T ENSP00000443671.1:p.Lys352Met
ENST00000597811.5:c.758A>T
NM_006297.2:c.1148A>T , LRG_784t1:c.1148A>T NP_006288.2:p.Lys383Met
NM_006297.3:c.1148A>T MANE Select NP_006288.2:p.Lys383Met