Canonical Allele Identifier: CA2011754882
Gene: RAD52 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.955370_955371delinsAT , CM000674.2:g.955370_955371delinsAT GRCh38
NC_000012.11:g.1064536_1064537delinsAT , CM000674.1:g.1064536_1064537delinsAT GRCh37
NC_000012.10:g.934797_934798delinsAT NCBI36
NG_017078.2:g.39671_39672delinsAT

Transcript Alleles

HGVS Amino-acid Change
ENST00000430095.6:c.-18-22295_-18-22294delinsAT ENSP00000387901.2:n.-18-22295_-18-22294delinsAT
NM_001297419.1:c.-18-22295_-18-22294delinsAT NP_001284348.1:n.-18-22295_-18-22294delinsAT
XM_005253720.3:c.-18-22295_-18-22294delinsAT XP_005253777.1:n.-18-22295_-18-22294delinsAT
XM_005253720.5:c.-18-22295_-18-22294delinsAT XP_005253777.1:n.-18-22295_-18-22294delinsAT
XM_017019769.1:c.-18-22295_-18-22294delinsAT XP_016875258.1:n.-18-22295_-18-22294delinsAT
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