Canonical Allele Identifier: CA406203348

Gene: XRCC1

Linked Data

• dbSNP Id: rs2146048949
• MyVariant Identifiers: chr19:g.44055767C>G (hg19) ; chr19:g.43551615C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.43551615C>G , CM000681.2:g.43551615C>G	GRCh38
NC_000019.9:g.44055767C>G , CM000681.1:g.44055767C>G	GRCh37
NC_000019.8:g.48747607C>G	NCBI36
NG_033799.1:g.28964G>C , LRG_784:g.28964G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262887.10:c.1155G>C MANE Select	ENSP00000262887.5:p.Trp385Cys
ENST00000262887.9:c.1155G>C	ENSP00000262887.4:p.Trp385Cys
ENST00000543982.5:c.1062G>C	ENSP00000443671.1:p.Trp354Cys
ENST00000597811.5:c.765G>C
NM_006297.2:c.1155G>C , LRG_784t1:c.1155G>C	NP_006288.2:p.Trp385Cys
NM_006297.3:c.1155G>C MANE Select	NP_006288.2:p.Trp385Cys