Canonical Allele Identifier: CA943969576
Gene: RAD52 HGNC NCBI

Linked Data

dbSNP Id: rs1958589861
gnomAD v3: 12-955372-CTG-C
gnomAD v4: 12-955372-CTG-C
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.955374_955375del , CM000674.2:g.955374_955375del GRCh38
NC_000012.11:g.1064540_1064541del , CM000674.1:g.1064540_1064541del GRCh37
NC_000012.10:g.934801_934802del NCBI36
NG_017078.2:g.39668_39669del

Transcript Alleles

HGVS Amino-acid Change
ENST00000430095.6:c.-18-22298_-18-22297del ENSP00000387901.2:n.-18-22298_-18-22297del
NM_001297419.1:c.-18-22298_-18-22297del NP_001284348.1:n.-18-22298_-18-22297del
XM_005253720.3:c.-18-22298_-18-22297del XP_005253777.1:n.-18-22298_-18-22297del
XM_005253720.5:c.-18-22298_-18-22297del XP_005253777.1:n.-18-22298_-18-22297del
XM_017019769.1:c.-18-22298_-18-22297del XP_016875258.1:n.-18-22298_-18-22297del
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