Canonical Allele Identifier: CA507741184
Gene: XRCC1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr19:g.44056318A>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.43552166A>T , CM000681.2:g.43552166A>T GRCh38
NC_000019.9:g.44056318A>T , CM000681.1:g.44056318A>T GRCh37
NC_000019.8:g.48748158A>T NCBI36
NG_033799.1:g.28413T>A , LRG_784:g.28413T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000262887.10:c.933T>A MANE Select ENSP00000262887.5:p.Ala311=
ENST00000262887.9:c.933T>A ENSP00000262887.4:p.Ala311=
ENST00000543982.5:c.840T>A ENSP00000443671.1:p.Ala280=
ENST00000595789.5:n.1054T>A
ENST00000597811.5:c.543T>A
ENST00000598422.1:n.613T>A
NM_006297.2:c.933T>A , LRG_784t1:c.933T>A NP_006288.2:p.Ala311=
NM_006297.3:c.933T>A MANE Select NP_006288.2:p.Ala311=