Canonical Allele Identifier: CA406203526

Gene: XRCC1

Linked Data

• dbSNP Id: rs2146049098
• MyVariant Identifiers: chr19:g.44055798C>T (hg19) ; chr19:g.43551646C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.43551646C>T , CM000681.2:g.43551646C>T	GRCh38
NC_000019.9:g.44055798C>T , CM000681.1:g.44055798C>T	GRCh37
NC_000019.8:g.48747638C>T	NCBI36
NG_033799.1:g.28933G>A , LRG_784:g.28933G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262887.10:c.1124G>A MANE Select	ENSP00000262887.5:p.Gly375Asp
ENST00000262887.9:c.1124G>A	ENSP00000262887.4:p.Gly375Asp
ENST00000543982.5:c.1031G>A	ENSP00000443671.1:p.Gly344Asp
ENST00000597811.5:c.734G>A
NM_006297.2:c.1124G>A , LRG_784t1:c.1124G>A	NP_006288.2:p.Gly375Asp
NM_006297.3:c.1124G>A MANE Select	NP_006288.2:p.Gly375Asp