Canonical Allele Identifier: CA406203366
Gene: XRCC1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr19:g.44055769A>G (hg19) chr19:g.43551617A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.43551617A>G , CM000681.2:g.43551617A>G GRCh38
NC_000019.9:g.44055769A>G , CM000681.1:g.44055769A>G GRCh37
NC_000019.8:g.48747609A>G NCBI36
NG_033799.1:g.28962T>C , LRG_784:g.28962T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000262887.10:c.1153T>C MANE Select ENSP00000262887.5:p.Trp385Arg
ENST00000262887.9:c.1153T>C ENSP00000262887.4:p.Trp385Arg
ENST00000543982.5:c.1060T>C ENSP00000443671.1:p.Trp354Arg
ENST00000597811.5:c.763T>C
NM_006297.2:c.1153T>C , LRG_784t1:c.1153T>C NP_006288.2:p.Trp385Arg
NM_006297.3:c.1153T>C MANE Select NP_006288.2:p.Trp385Arg
Search 100 bp 5'
Search 100 bp 3'