Canonical Allele Identifier: CA406203547
Gene: XRCC1 HGNC NCBI

Linked Data

dbSNP Id: rs2146049130

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.43551652A>T , CM000681.2:g.43551652A>T GRCh38
NC_000019.9:g.44055804A>T , CM000681.1:g.44055804A>T GRCh37
NC_000019.8:g.48747644A>T NCBI36
NG_033799.1:g.28927T>A , LRG_784:g.28927T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000262887.10:c.1118T>A MANE Select ENSP00000262887.5:p.Val373Asp
ENST00000262887.9:c.1118T>A ENSP00000262887.4:p.Val373Asp
ENST00000543982.5:c.1025T>A ENSP00000443671.1:p.Val342Asp
ENST00000597811.5:c.728T>A
NM_006297.2:c.1118T>A , LRG_784t1:c.1118T>A NP_006288.2:p.Val373Asp
NM_006297.3:c.1118T>A MANE Select NP_006288.2:p.Val373Asp