Canonical Allele Identifier: CA712760226

Gene: RAD51

Linked Data

• dbSNP Id: rs1250978972
• gnomAD v3: 15-40695337-T-TG
• gnomAD v4: 15-40695337-T-TG
• MyVariant Identifiers: chr15:g.40987535_40987536insG (hg19) ; chr15:g.40695337_40695338insG (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.40695342dup , CM000677.2:g.40695342dup	GRCh38
NC_000015.9:g.40987540dup , CM000677.1:g.40987540dup	GRCh37
NC_000015.8:g.38774832dup	NCBI36
NG_012120.1:g.5182dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000267868.8:c.-86dup MANE Select	ENSP00000267868.3:n.-86dup
ENST00000645673.2:c.-86dup	ENSP00000493712.2:n.-86dup
ENST00000267868.7:c.-86dup	ENSP00000267868.3:n.-86dup
ENST00000382643.7:c.-3+21dup	ENSP00000372088.3:n.-3+21dup
ENST00000423169.6:c.-86dup	ENSP00000406602.2:n.-86dup
ENST00000525066.5:c.-86dup	ENSP00000431864.1:n.-86dup
ENST00000527860.5:c.-3+522dup	ENSP00000432759.1:n.-3+522dup
ENST00000532743.5:c.-86dup	ENSP00000433924.1:n.-86dup
ENST00000557850.5:c.-86dup	ENSP00000454176.1:n.-86dup
NM_001164269.1:c.-3+21dup	NP_001157741.1:n.-3+21dup
NM_001164270.1:c.-86dup	NP_001157742.1:n.-86dup
NM_002875.4:c.-86dup	NP_002866.2:n.-86dup
NM_133487.3:c.-86dup	NP_597994.3:n.-86dup
XM_011521857.1:c.-3+522dup	XP_011520159.1:n.-3+522dup
XM_011521860.1:c.-3+21dup	XP_011520162.1:n.-3+21dup
XM_011521861.1:c.-3+522dup	XP_011520163.1:n.-3+522dup
XM_011521862.1:c.-340dup	XP_011520164.1:n.-340dup
XM_011521857.2:c.-3+522dup	XP_011520159.1:n.-3+522dup
XM_011521860.2:c.-3+21dup	XP_011520162.1:n.-3+21dup
XM_011521861.2:c.-3+522dup	XP_011520163.1:n.-3+522dup
XM_011521862.3:c.-340dup	XP_011520164.1:n.-340dup
NM_001164269.2:c.-3+21dup	NP_001157741.1:n.-3+21dup
NM_001164270.2:c.-86dup	NP_001157742.1:n.-86dup
NM_002875.5:c.-86dup MANE Select	NP_002866.2:n.-86dup
NM_133487.4:c.-86dup	NP_597994.3:n.-86dup