Canonical Allele Identifier: CA406203315
Gene: XRCC1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr19:g.44055759T>G (hg19) chr19:g.43551607T>G (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.43551607T>G , CM000681.2:g.43551607T>G GRCh38
NC_000019.9:g.44055759T>G , CM000681.1:g.44055759T>G GRCh37
NC_000019.8:g.48747599T>G NCBI36
NG_033799.1:g.28972A>C , LRG_784:g.28972A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000262887.10:c.1163A>C MANE Select ENSP00000262887.5:p.Asp388Ala
ENST00000262887.9:c.1163A>C ENSP00000262887.4:p.Asp388Ala
ENST00000543982.5:c.1070A>C ENSP00000443671.1:p.Asp357Ala
ENST00000597811.5:c.773A>C
NM_006297.2:c.1163A>C , LRG_784t1:c.1163A>C NP_006288.2:p.Asp388Ala
NM_006297.3:c.1163A>C MANE Select NP_006288.2:p.Asp388Ala
Search 100 bp 5'
Search 100 bp 3'