Canonical Allele Identifier: CA406203285

Gene: XRCC1

Linked Data

• dbSNP Id: rs1356332197
• MyVariant Identifiers: chr19:g.44055753T>G (hg19) ; chr19:g.43551601T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.43551601T>G , CM000681.2:g.43551601T>G	GRCh38
NC_000019.9:g.44055753T>G , CM000681.1:g.44055753T>G	GRCh37
NC_000019.8:g.48747593T>G	NCBI36
NG_033799.1:g.28978A>C , LRG_784:g.28978A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262887.10:c.1169A>C MANE Select	ENSP00000262887.5:p.His390Pro
ENST00000262887.9:c.1169A>C	ENSP00000262887.4:p.His390Pro
ENST00000543982.5:c.1076A>C	ENSP00000443671.1:p.His359Pro
ENST00000597811.5:c.779A>C
NM_006297.2:c.1169A>C , LRG_784t1:c.1169A>C	NP_006288.2:p.His390Pro
NM_006297.3:c.1169A>C MANE Select	NP_006288.2:p.His390Pro