Canonical Allele Identifier: CA996142429
Gene: XRCC1 HGNC NCBI

Linked Data

dbSNP Id: rs55974714

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.43551776_43551779del , CM000681.2:g.43551776_43551779del GRCh38
NC_000019.9:g.44055928_44055931del , CM000681.1:g.44055928_44055931del GRCh37
NC_000019.8:g.48747768_48747771del NCBI36
NG_033799.1:g.28811_28814del , LRG_784:g.28811_28814del

Transcript Alleles

HGVS Amino-acid Change
ENST00000262887.10:c.1083-81_1083-78del MANE Select ENSP00000262887.5:n.1083-81_1083-78del
ENST00000262887.9:c.1083-81_1083-78del ENSP00000262887.4:n.1083-81_1083-78del
ENST00000543982.5:c.990-81_990-78del ENSP00000443671.1:n.990-81_990-78del
ENST00000597811.5:c.693-81_693-78del
NM_006297.2:c.1083-81_1083-78del , LRG_784t1:c.1083-81_1083-78del NP_006288.2:n.1083-81_1083-78del
NM_006297.3:c.1083-81_1083-78del MANE Select NP_006288.2:n.1083-81_1083-78del