Canonical Allele Identifier: CA693673539

Gene: RAD52

Linked Data

• dbSNP Id: rs1254514955
• gnomAD v4: 12-955091-TA-T
• MyVariant Identifiers: chr12:g.1064258del (hg19) ; chr12:g.955092del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.955094del , CM000674.2:g.955094del	GRCh38
NC_000012.11:g.1064260del , CM000674.1:g.1064260del	GRCh37
NC_000012.10:g.934521del	NCBI36
NG_017078.2:g.39950del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000430095.6:c.-18-22016del	ENSP00000387901.2:n.-18-22016del
NM_001297419.1:c.-18-22016del	NP_001284348.1:n.-18-22016del
XM_005253720.3:c.-18-22016del	XP_005253777.1:n.-18-22016del
XM_005253720.5:c.-18-22016del	XP_005253777.1:n.-18-22016del
XM_017019769.1:c.-18-22016del	XP_016875258.1:n.-18-22016del