Canonical Allele Identifier: CA14662229

Gene: XRCC1

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.43570445T>G , CM000681.2:g.43570445T>G	GRCh38
NC_000019.9:g.44074597T>G , CM000681.1:g.44074597T>G	GRCh37
NC_000019.8:g.48766437T>G	NCBI36
NG_033799.1:g.10134A>C , LRG_784:g.10134A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262887.10:c.144+4465A>C MANE Select	ENSP00000262887.5:n.144+4465A>C
ENST00000262887.9:c.144+4465A>C	ENSP00000262887.4:n.144+4465A>C
ENST00000543982.5:c.51+4963A>C	ENSP00000443671.1:n.51+4963A>C
ENST00000594107.1:c.144+4465A>C	ENSP00000471159.1:n.144+4465A>C
ENST00000594374.1:c.170-9425A>C
ENST00000595789.5:n.192+4465A>C
ENST00000598165.5:c.165+4465A>C	ENSP00000470045.1:n.165+4465A>C
ENST00000599693.5:c.71-9425A>C
NM_006297.2:c.144+4465A>C , LRG_784t1:c.144+4465A>C	NP_006288.2:n.144+4465A>C
NM_006297.3:c.144+4465A>C MANE Select	NP_006288.2:n.144+4465A>C