Canonical Allele Identifier: CA943969552
Gene: RAD52 HGNC NCBI

Linked Data

dbSNP Id: rs1958587149

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.955160_955162del , CM000674.2:g.955160_955162del GRCh38
NC_000012.11:g.1064326_1064328del , CM000674.1:g.1064326_1064328del GRCh37
NC_000012.10:g.934587_934589del NCBI36
NG_017078.2:g.39883_39885del

Transcript Alleles

HGVS Amino-acid Change
ENST00000430095.6:c.-18-22083_-18-22081del ENSP00000387901.2:n.-18-22083_-18-22081del
NM_001297419.1:c.-18-22083_-18-22081del NP_001284348.1:n.-18-22083_-18-22081del
XM_005253720.3:c.-18-22083_-18-22081del XP_005253777.1:n.-18-22083_-18-22081del
XM_005253720.5:c.-18-22083_-18-22081del XP_005253777.1:n.-18-22083_-18-22081del
XM_017019769.1:c.-18-22083_-18-22081del XP_016875258.1:n.-18-22083_-18-22081del