Canonical Allele Identifier: CA996142464
Gene: XRCC1 HGNC NCBI

Linked Data

dbSNP Id: rs1972579019

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.43551832G>A , CM000681.2:g.43551832G>A GRCh38
NC_000019.9:g.44055984G>A , CM000681.1:g.44055984G>A GRCh37
NC_000019.8:g.48747824G>A NCBI36
NG_033799.1:g.28747C>T , LRG_784:g.28747C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000262887.10:c.1083-145C>T MANE Select ENSP00000262887.5:n.1083-145C>T
ENST00000262887.9:c.1083-145C>T ENSP00000262887.4:n.1083-145C>T
ENST00000543982.5:c.990-145C>T ENSP00000443671.1:n.990-145C>T
ENST00000597811.5:c.693-145C>T
NM_006297.2:c.1083-145C>T , LRG_784t1:c.1083-145C>T NP_006288.2:n.1083-145C>T
NM_006297.3:c.1083-145C>T MANE Select NP_006288.2:n.1083-145C>T