Canonical Allele Identifier: CA507741033

Gene: XRCC1

Linked Data

• MyVariant Identifiers: chr19:g.44055776A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.43551624A>C , CM000681.2:g.43551624A>C	GRCh38
NC_000019.9:g.44055776A>C , CM000681.1:g.44055776A>C	GRCh37
NC_000019.8:g.48747616A>C	NCBI36
NG_033799.1:g.28955T>G , LRG_784:g.28955T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262887.10:c.1146T>G MANE Select	ENSP00000262887.5:p.Arg382=
ENST00000262887.9:c.1146T>G	ENSP00000262887.4:p.Arg382=
ENST00000543982.5:c.1053T>G	ENSP00000443671.1:p.Arg351=
ENST00000597811.5:c.756T>G
NM_006297.2:c.1146T>G , LRG_784t1:c.1146T>G	NP_006288.2:p.Arg382=
NM_006297.3:c.1146T>G MANE Select	NP_006288.2:p.Arg382=