Canonical Allele Identifier: CA882548952

Gene: XRCC1

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.43557785T>C , CM000681.2:g.43557785T>C	GRCh38
NC_000019.9:g.44061937T>C , CM000681.1:g.44061937T>C	GRCh37
NC_000019.8:g.48753777T>C	NCBI36
NG_033799.1:g.22794A>G , LRG_784:g.22794A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262887.10:c.256-2981A>G MANE Select	ENSP00000262887.5:n.256-2981A>G
ENST00000262887.9:c.256-2981A>G	ENSP00000262887.4:n.256-2981A>G
ENST00000543982.5:c.163-2981A>G	ENSP00000443671.1:n.163-2981A>G
ENST00000594107.1:c.145-2981A>G	ENSP00000471159.1:n.145-2981A>G
ENST00000594374.1:c.281-2981A>G
ENST00000595789.5:n.304-2981A>G
ENST00000597811.5:c.41-2981A>G
ENST00000598165.5:c.277-2981A>G	ENSP00000470045.1:n.277-2981A>G
ENST00000599693.5:c.182-2981A>G
NM_006297.2:c.256-2981A>G , LRG_784t1:c.256-2981A>G	NP_006288.2:n.256-2981A>G
NM_006297.3:c.256-2981A>G MANE Select	NP_006288.2:n.256-2981A>G