Canonical Allele Identifier: CA406203541
Gene: XRCC1 HGNC NCBI

Linked Data

dbSNP Id: rs1358353056

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.43551650G>T , CM000681.2:g.43551650G>T GRCh38
NC_000019.9:g.44055802G>T , CM000681.1:g.44055802G>T GRCh37
NC_000019.8:g.48747642G>T NCBI36
NG_033799.1:g.28929C>A , LRG_784:g.28929C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000262887.10:c.1120C>A MANE Select ENSP00000262887.5:p.Leu374Ile
ENST00000262887.9:c.1120C>A ENSP00000262887.4:p.Leu374Ile
ENST00000543982.5:c.1027C>A ENSP00000443671.1:p.Leu343Ile
ENST00000597811.5:c.730C>A
NM_006297.2:c.1120C>A , LRG_784t1:c.1120C>A NP_006288.2:p.Leu374Ile
NM_006297.3:c.1120C>A MANE Select NP_006288.2:p.Leu374Ile