Canonical Allele Identifier: CA2011754884
Gene: RAD52 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.955372_955374delinsCTG , CM000674.2:g.955372_955374delinsCTG GRCh38
NC_000012.11:g.1064538_1064540delinsCTG , CM000674.1:g.1064538_1064540delinsCTG GRCh37
NC_000012.10:g.934799_934801delinsCTG NCBI36
NG_017078.2:g.39668_39670delinsCAG

Transcript Alleles

HGVS Amino-acid change
ENST00000430095.6:c.-18-22298_-18-22296delinsCAG ENSP00000387901.2:n.-18-22298_-18-22296delinsCAG
NM_001297419.1:c.-18-22298_-18-22296delinsCAG NP_001284348.1:n.-18-22298_-18-22296delinsCAG
XM_005253720.3:c.-18-22298_-18-22296delinsCAG XP_005253777.1:n.-18-22298_-18-22296delinsCAG
XM_005253720.5:c.-18-22298_-18-22296delinsCAG XP_005253777.1:n.-18-22298_-18-22296delinsCAG
XM_017019769.1:c.-18-22298_-18-22296delinsCAG XP_016875258.1:n.-18-22298_-18-22296delinsCAG
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