Canonical Allele Identifier: CA406203379
Gene: XRCC1 HGNC NCBI

Linked Data

dbSNP Id: rs2146048971

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.43551619T>C , CM000681.2:g.43551619T>C GRCh38
NC_000019.9:g.44055771T>C , CM000681.1:g.44055771T>C GRCh37
NC_000019.8:g.48747611T>C NCBI36
NG_033799.1:g.28960A>G , LRG_784:g.28960A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000262887.10:c.1151A>G MANE Select ENSP00000262887.5:p.Glu384Gly
ENST00000262887.9:c.1151A>G ENSP00000262887.4:p.Glu384Gly
ENST00000543982.5:c.1058A>G ENSP00000443671.1:p.Glu353Gly
ENST00000597811.5:c.761A>G
NM_006297.2:c.1151A>G , LRG_784t1:c.1151A>G NP_006288.2:p.Glu384Gly
NM_006297.3:c.1151A>G MANE Select NP_006288.2:p.Glu384Gly