Canonical Allele Identifier: CA2011754832
Gene: RAD52 HGNC NCBI

Linked Data

dbSNP Id: rs1958588268

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.955243_955244insA , CM000674.2:g.955243_955244insA GRCh38
NC_000012.11:g.1064409_1064410insA , CM000674.1:g.1064409_1064410insA GRCh37
NC_000012.10:g.934670_934671insA NCBI36
NG_017078.2:g.39798_39799insT

Transcript Alleles

HGVS Amino-acid change
ENST00000430095.6:c.-18-22168_-18-22167insT ENSP00000387901.2:n.-18-22168_-18-22167in...
NM_001297419.1:c.-18-22168_-18-22167insT NP_001284348.1:n.-18-22168_-18-22167insT
XM_005253720.3:c.-18-22168_-18-22167insT XP_005253777.1:n.-18-22168_-18-22167insT
XM_005253720.5:c.-18-22168_-18-22167insT XP_005253777.1:n.-18-22168_-18-22167insT
XM_017019769.1:c.-18-22168_-18-22167insT XP_016875258.1:n.-18-22168_-18-22167insT