Canonical Allele Identifier: CA507741026

Gene: XRCC1

Linked Data

• dbSNP Id: rs199613843
• MyVariant Identifiers: chr19:g.44055761C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.43551609C>A , CM000681.2:g.43551609C>A	GRCh38
NC_000019.9:g.44055761C>A , CM000681.1:g.44055761C>A	GRCh37
NC_000019.8:g.48747601C>A	NCBI36
NG_033799.1:g.28970G>T , LRG_784:g.28970G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262887.10:c.1161G>T MANE Select	ENSP00000262887.5:p.Leu387=
ENST00000262887.9:c.1161G>T	ENSP00000262887.4:p.Leu387=
ENST00000543982.5:c.1068G>T	ENSP00000443671.1:p.Leu356=
ENST00000597811.5:c.771G>T
NM_006297.2:c.1161G>T , LRG_784t1:c.1161G>T	NP_006288.2:p.Leu387=
NM_006297.3:c.1161G>T MANE Select	NP_006288.2:p.Leu387=