Canonical Allele Identifier: CA712760267

Gene: RAD51

Linked Data

• dbSNP Id: rs1263625916
• gnomAD v3: 15-40695407-A-T
• gnomAD v4: 15-40695407-A-T
• MyVariant Identifiers: chr15:g.40987605A>T (hg19) ; chr15:g.40695407A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.40695407A>T , CM000677.2:g.40695407A>T	GRCh38
NC_000015.9:g.40987605A>T , CM000677.1:g.40987605A>T	GRCh37
NC_000015.8:g.38774897A>T	NCBI36
NG_012120.1:g.5247A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000267868.8:c.-21A>T MANE Select	ENSP00000267868.3:n.-21A>T
ENST00000645673.2:c.-21A>T	ENSP00000493712.2:n.-21A>T
ENST00000267868.7:c.-21A>T	ENSP00000267868.3:n.-21A>T
ENST00000382643.7:c.-3+86A>T	ENSP00000372088.3:n.-3+86A>T
ENST00000423169.6:c.-21A>T	ENSP00000406602.2:n.-21A>T
ENST00000525066.5:c.-21A>T	ENSP00000431864.1:n.-21A>T
ENST00000527860.5:c.-3+587A>T	ENSP00000432759.1:n.-3+587A>T
ENST00000532743.5:c.-21A>T	ENSP00000433924.1:n.-21A>T
ENST00000557850.5:c.-21A>T	ENSP00000454176.1:n.-21A>T
NM_001164269.1:c.-3+86A>T	NP_001157741.1:n.-3+86A>T
NM_001164270.1:c.-21A>T	NP_001157742.1:n.-21A>T
NM_002875.4:c.-21A>T	NP_002866.2:n.-21A>T
NM_133487.3:c.-21A>T	NP_597994.3:n.-21A>T
XM_011521857.1:c.-3+587A>T	XP_011520159.1:n.-3+587A>T
XM_011521860.1:c.-3+86A>T	XP_011520162.1:n.-3+86A>T
XM_011521861.1:c.-3+587A>T	XP_011520163.1:n.-3+587A>T
XM_011521862.1:c.-275A>T	XP_011520164.1:n.-275A>T
XM_011521857.2:c.-3+587A>T	XP_011520159.1:n.-3+587A>T
XM_011521860.2:c.-3+86A>T	XP_011520162.1:n.-3+86A>T
XM_011521861.2:c.-3+587A>T	XP_011520163.1:n.-3+587A>T
XM_011521862.3:c.-275A>T	XP_011520164.1:n.-275A>T
NM_001164269.2:c.-3+86A>T	NP_001157741.1:n.-3+86A>T
NM_001164270.2:c.-21A>T	NP_001157742.1:n.-21A>T
NM_002875.5:c.-21A>T MANE Select	NP_002866.2:n.-21A>T
NM_133487.4:c.-21A>T	NP_597994.3:n.-21A>T