Canonical Allele Identifier: CA406203386

Gene: XRCC1

Linked Data

• dbSNP Id: rs1178861239
• MyVariant Identifiers: chr19:g.44055772C>T (hg19) ; chr19:g.43551620C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.43551620C>T , CM000681.2:g.43551620C>T	GRCh38
NC_000019.9:g.44055772C>T , CM000681.1:g.44055772C>T	GRCh37
NC_000019.8:g.48747612C>T	NCBI36
NG_033799.1:g.28959G>A , LRG_784:g.28959G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262887.10:c.1150G>A MANE Select	ENSP00000262887.5:p.Glu384Lys
ENST00000262887.9:c.1150G>A	ENSP00000262887.4:p.Glu384Lys
ENST00000543982.5:c.1057G>A	ENSP00000443671.1:p.Glu353Lys
ENST00000597811.5:c.760G>A
NM_006297.2:c.1150G>A , LRG_784t1:c.1150G>A	NP_006288.2:p.Glu384Lys
NM_006297.3:c.1150G>A MANE Select	NP_006288.2:p.Glu384Lys