Canonical Allele Identifier: CA406203522
Gene: XRCC1 HGNC NCBI

Linked Data

dbSNP Id: rs2146049098

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.43551646C>A , CM000681.2:g.43551646C>A GRCh38
NC_000019.9:g.44055798C>A , CM000681.1:g.44055798C>A GRCh37
NC_000019.8:g.48747638C>A NCBI36
NG_033799.1:g.28933G>T , LRG_784:g.28933G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000262887.10:c.1124G>T MANE Select ENSP00000262887.5:p.Gly375Val
ENST00000262887.9:c.1124G>T ENSP00000262887.4:p.Gly375Val
ENST00000543982.5:c.1031G>T ENSP00000443671.1:p.Gly344Val
ENST00000597811.5:c.734G>T
NM_006297.2:c.1124G>T , LRG_784t1:c.1124G>T NP_006288.2:p.Gly375Val
NM_006297.3:c.1124G>T MANE Select NP_006288.2:p.Gly375Val