Canonical Allele Identifier: CA406203383

Gene: XRCC1

Linked Data

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

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262887.10:c.1150G>T MANE Select	ENSP00000262887.5:p.Glu384Ter
ENST00000262887.9:c.1150G>T	ENSP00000262887.4:p.Glu384Ter
ENST00000543982.5:c.1057G>T	ENSP00000443671.1:p.Glu353Ter
ENST00000597811.5:c.760G>T
NM_006297.2:c.1150G>T , LRG_784t1:c.1150G>T	NP_006288.2:p.Glu384Ter
NM_006297.3:c.1150G>T MANE Select	NP_006288.2:p.Glu384Ter