Canonical Allele Identifier: CA693750145

Gene: RAD52

Linked Data

• dbSNP Id: rs1281542188
• MyVariant Identifiers: chr12:g.1064537del (hg19) ; chr12:g.955371del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.955371del , CM000674.2:g.955371del	GRCh38
NC_000012.11:g.1064537del , CM000674.1:g.1064537del	GRCh37
NC_000012.10:g.934798del	NCBI36
NG_017078.2:g.39671del

Transcript Alleles

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