Canonical Allele Identifier: CA406203433

Gene: XRCC1

Linked Data

• dbSNP Id: rs759332835
• MyVariant Identifiers: chr19:g.44055780A>G (hg19) ; chr19:g.43551628A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.43551628A>G , CM000681.2:g.43551628A>G	GRCh38
NC_000019.9:g.44055780A>G , CM000681.1:g.44055780A>G	GRCh37
NC_000019.8:g.48747620A>G	NCBI36
NG_033799.1:g.28951T>C , LRG_784:g.28951T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262887.10:c.1142T>C MANE Select	ENSP00000262887.5:p.Val381Ala
ENST00000262887.9:c.1142T>C	ENSP00000262887.4:p.Val381Ala
ENST00000543982.5:c.1049T>C	ENSP00000443671.1:p.Val350Ala
ENST00000597811.5:c.752T>C
NM_006297.2:c.1142T>C , LRG_784t1:c.1142T>C	NP_006288.2:p.Val381Ala
NM_006297.3:c.1142T>C MANE Select	NP_006288.2:p.Val381Ala