Canonical Allele Identifier: CA406207288

Gene: XRCC1

Linked Data

• dbSNP Id: rs1799782
• MyVariant Identifiers: chr19:g.44057574G>C (hg19) ; chr19:g.43553422G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.43553422G>C , CM000681.2:g.43553422G>C	GRCh38
NC_000019.9:g.44057574G>C , CM000681.1:g.44057574G>C	GRCh37
NC_000019.8:g.48749414G>C	NCBI36
NG_033799.1:g.27157C>G , LRG_784:g.27157C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000262887.10:c.580C>G MANE Select	ENSP00000262887.5:p.Arg194Gly
ENST00000262887.9:c.580C>G	ENSP00000262887.4:p.Arg194Gly
ENST00000543982.5:c.487C>G	ENSP00000443671.1:p.Arg163Gly
ENST00000594107.1:c.469C>G	ENSP00000471159.1:p.Arg157Gly
ENST00000595789.5:n.628C>G
ENST00000597811.5:c.365C>G
ENST00000598165.5:c.601C>G	ENSP00000470045.1:p.Arg201Gly
ENST00000598422.1:n.260C>G
ENST00000599693.5:c.506C>G
NM_006297.2:c.580C>G , LRG_784t1:c.580C>G	NP_006288.2:p.Arg194Gly
NM_006297.3:c.580C>G MANE Select	NP_006288.2:p.Arg194Gly