Canonical Allele Identifier: CA406204963

Gene: XRCC1

Linked Data

• MyVariant Identifiers: chr19:g.44056316C>G (hg19) ; chr19:g.43552164C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.43552164C>G , CM000681.2:g.43552164C>G	GRCh38
NC_000019.9:g.44056316C>G , CM000681.1:g.44056316C>G	GRCh37
NC_000019.8:g.48748156C>G	NCBI36
NG_033799.1:g.28415G>C , LRG_784:g.28415G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262887.10:c.935G>C MANE Select	ENSP00000262887.5:p.Gly312Ala
ENST00000262887.9:c.935G>C	ENSP00000262887.4:p.Gly312Ala
ENST00000543982.5:c.842G>C	ENSP00000443671.1:p.Gly281Ala
ENST00000595789.5:n.1056G>C
ENST00000597811.5:c.545G>C
ENST00000598422.1:n.615G>C
NM_006297.2:c.935G>C , LRG_784t1:c.935G>C	NP_006288.2:p.Gly312Ala
NM_006297.3:c.935G>C MANE Select	NP_006288.2:p.Gly312Ala