Canonical Allele Identifier: CA308773747
Gene: XRCC1 HGNC NCBI

Linked Data

dbSNP Id: rs919928068
gnomAD v3: 19-43551890-GA-G
gnomAD v4: 19-43551890-GA-G
MyVariant Identifiers: chr19:g.44056043del (hg19) chr19:g.43551891del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.43551893del , CM000681.2:g.43551893del GRCh38
NC_000019.9:g.44056045del , CM000681.1:g.44056045del GRCh37
NC_000019.8:g.48747885del NCBI36
NG_033799.1:g.28688del , LRG_784:g.28688del

Transcript Alleles

HGVS Amino-acid Change
ENST00000262887.10:c.1082+126del MANE Select ENSP00000262887.5:n.1082+126del
ENST00000262887.9:c.1082+126del ENSP00000262887.4:n.1082+126del
ENST00000543982.5:c.989+126del ENSP00000443671.1:n.989+126del
ENST00000597811.5:c.692+126del
NM_006297.2:c.1082+126del , LRG_784t1:c.1082+126del NP_006288.2:n.1082+126del
NM_006297.3:c.1082+126del MANE Select NP_006288.2:n.1082+126del
Search 100 bp 5'
Search 100 bp 3'