Canonical Allele Identifier: CA406203476
Gene: XRCC1 HGNC NCBI

Linked Data

dbSNP Id: rs2146049053

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.43551637C>G , CM000681.2:g.43551637C>G GRCh38
NC_000019.9:g.44055789C>G , CM000681.1:g.44055789C>G GRCh37
NC_000019.8:g.48747629C>G NCBI36
NG_033799.1:g.28942G>C , LRG_784:g.28942G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000262887.10:c.1133G>C MANE Select ENSP00000262887.5:p.Gly378Ala
ENST00000262887.9:c.1133G>C ENSP00000262887.4:p.Gly378Ala
ENST00000543982.5:c.1040G>C ENSP00000443671.1:p.Gly347Ala
ENST00000597811.5:c.743G>C
NM_006297.2:c.1133G>C , LRG_784t1:c.1133G>C NP_006288.2:p.Gly378Ala
NM_006297.3:c.1133G>C MANE Select NP_006288.2:p.Gly378Ala