Canonical Allele Identifier: CA507741189
Gene: XRCC1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr19:g.44056324G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.43552172G>A , CM000681.2:g.43552172G>A GRCh38
NC_000019.9:g.44056324G>A , CM000681.1:g.44056324G>A GRCh37
NC_000019.8:g.48748164G>A NCBI36
NG_033799.1:g.28407C>T , LRG_784:g.28407C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000262887.10:c.927C>T MANE Select ENSP00000262887.5:p.Pro309=
ENST00000262887.9:c.927C>T ENSP00000262887.4:p.Pro309=
ENST00000543982.5:c.834C>T ENSP00000443671.1:p.Pro278=
ENST00000595789.5:n.1048C>T
ENST00000597811.5:c.537C>T
ENST00000598422.1:n.607C>T
NM_006297.2:c.927C>T , LRG_784t1:c.927C>T NP_006288.2:p.Pro309=
NM_006297.3:c.927C>T MANE Select NP_006288.2:p.Pro309=