Canonical Allele Identifier: CA507741040

Gene: XRCC1

Linked Data

• dbSNP Id: rs368206391
• MyVariant Identifiers: chr19:g.44055785G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.43551633G>T , CM000681.2:g.43551633G>T	GRCh38
NC_000019.9:g.44055785G>T , CM000681.1:g.44055785G>T	GRCh37
NC_000019.8:g.48747625G>T	NCBI36
NG_033799.1:g.28946C>A , LRG_784:g.28946C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262887.10:c.1137C>A MANE Select	ENSP00000262887.5:p.Arg379=
ENST00000262887.9:c.1137C>A	ENSP00000262887.4:p.Arg379=
ENST00000543982.5:c.1044C>A	ENSP00000443671.1:p.Arg348=
ENST00000597811.5:c.747C>A
NM_006297.2:c.1137C>A , LRG_784t1:c.1137C>A	NP_006288.2:p.Arg379=
NM_006297.3:c.1137C>A MANE Select	NP_006288.2:p.Arg379=