Canonical Allele Identifier: CA882544450
Gene: XRCC1 HGNC NCBI

Linked Data

dbSNP Id: rs1223671393
gnomAD v3: 19-43551850-C-CA
gnomAD v4: 19-43551850-C-CA
MyVariant Identifiers: chr19:g.44056002_44056003insA (hg19) chr19:g.43551850_43551851insA (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.43551855dup , CM000681.2:g.43551855dup GRCh38
NC_000019.9:g.44056007dup , CM000681.1:g.44056007dup GRCh37
NC_000019.8:g.48747847dup NCBI36
NG_033799.1:g.28728dup , LRG_784:g.28728dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000262887.10:c.1083-164dup MANE Select ENSP00000262887.5:n.1083-164dup
ENST00000262887.9:c.1083-164dup ENSP00000262887.4:n.1083-164dup
ENST00000543982.5:c.990-164dup ENSP00000443671.1:n.990-164dup
ENST00000597811.5:c.693-164dup
NM_006297.2:c.1083-164dup , LRG_784t1:c.1083-164dup NP_006288.2:n.1083-164dup
NM_006297.3:c.1083-164dup MANE Select NP_006288.2:n.1083-164dup
Search 100 bp 5'
Search 100 bp 3'