Canonical Allele Identifier: CA2011754828
Gene: RAD52 HGNC NCBI

Linked Data

dbSNP Id: rs1958588227

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.955239_955240del , CM000674.2:g.955239_955240del GRCh38
NC_000012.11:g.1064405_1064406del , CM000674.1:g.1064405_1064406del GRCh37
NC_000012.10:g.934666_934667del NCBI36
NG_017078.2:g.39802_39803del

Transcript Alleles

HGVS Amino-acid change
ENST00000430095.6:c.-18-22164_-18-22163del ENSP00000387901.2:n.-18-22164_-18-22163de...
NM_001297419.1:c.-18-22164_-18-22163del NP_001284348.1:n.-18-22164_-18-22163del
XM_005253720.3:c.-18-22164_-18-22163del XP_005253777.1:n.-18-22164_-18-22163del
XM_005253720.5:c.-18-22164_-18-22163del XP_005253777.1:n.-18-22164_-18-22163del
XM_017019769.1:c.-18-22164_-18-22163del XP_016875258.1:n.-18-22164_-18-22163del