Canonical Allele Identifier: CA406203436
Gene: XRCC1 HGNC NCBI

Linked Data

dbSNP Id: rs2271980

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.43551629C>A , CM000681.2:g.43551629C>A GRCh38
NC_000019.9:g.44055781C>A , CM000681.1:g.44055781C>A GRCh37
NC_000019.8:g.48747621C>A NCBI36
NG_033799.1:g.28950G>T , LRG_784:g.28950G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000262887.10:c.1141G>T MANE Select ENSP00000262887.5:p.Val381Leu
ENST00000262887.9:c.1141G>T ENSP00000262887.4:p.Val381Leu
ENST00000543982.5:c.1048G>T ENSP00000443671.1:p.Val350Leu
ENST00000597811.5:c.751G>T
NM_006297.2:c.1141G>T , LRG_784t1:c.1141G>T NP_006288.2:p.Val381Leu
NM_006297.3:c.1141G>T MANE Select NP_006288.2:p.Val381Leu