Canonical Allele Identifier: CA391759198

Gene: RAD51

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.40729609G>A , CM000677.2:g.40729609G>A	GRCh38
NC_000015.9:g.41021807G>A , CM000677.1:g.41021807G>A	GRCh37
NC_000015.8:g.38809099G>A	NCBI36
NG_012120.1:g.39449G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_002875.5:c.749G>A MANE Select	NP_002866.2:p.Arg250Gln
ENST00000267868.8:c.749G>A MANE Select	ENSP00000267868.3:p.Arg250Gln
NM_001164269.1:c.752G>A	NP_001157741.1:p.Arg251Gln
NM_001164269.2:c.752G>A	NP_001157741.1:p.Arg251Gln
NM_001164270.1:c.749G>A	NP_001157742.1:p.Arg250Gln
NM_001164270.2:c.749G>A	NP_001157742.1:p.Arg250Gln
NM_002875.4:c.749G>A	NP_002866.2:p.Arg250Gln
NM_133487.3:c.752G>A	NP_597994.3:p.Arg251Gln
NM_133487.4:c.752G>A	NP_597994.3:p.Arg251Gln
ENST00000267868.7:c.749G>A	ENSP00000267868.3:p.Arg250Gln
ENST00000382643.7:c.752G>A	ENSP00000372088.3:p.Arg251Gln
ENST00000423169.6:c.749G>A	ENSP00000406602.2:p.Arg250Gln
ENST00000525066.5:c.*198G>A	ENSP00000431864.1:n.*198G>A
ENST00000531277.2:c.*328G>A	ENSP00000436512.2:n.*328G>A
ENST00000532743.5:c.752G>A	ENSP00000433924.1:p.Arg251Gln
ENST00000532743.6:c.749G>A	ENSP00000433924.2:p.Arg250Gln
ENST00000557850.5:c.458G>A	ENSP00000454176.1:p.Arg153Gln
ENST00000645673.2:c.752G>A	ENSP00000493712.2:p.Arg251Gln
XM_006720626.2:c.749G>A	XP_006720689.1:p.Arg250Gln
XM_006720626.3:c.749G>A	XP_006720689.1:p.Arg250Gln
XM_011521857.1:c.749G>A	XP_011520159.1:p.Arg250Gln
XM_011521857.2:c.749G>A	XP_011520159.1:p.Arg250Gln
XM_011521858.1:c.749G>A	XP_011520160.1:p.Arg250Gln
XM_011521858.2:c.749G>A	XP_011520160.1:p.Arg250Gln
XM_011521859.1:c.749G>A	XP_011520161.1:p.Arg250Gln
XM_011521859.2:c.749G>A	XP_011520161.1:p.Arg250Gln
XM_011521860.1:c.749G>A	XP_011520162.1:p.Arg250Gln
XM_011521860.2:c.749G>A	XP_011520162.1:p.Arg250Gln
XM_011521861.1:c.749G>A	XP_011520163.1:p.Arg250Gln
XM_011521861.2:c.749G>A	XP_011520163.1:p.Arg250Gln
XM_011521862.1:c.377G>A	XP_011520164.1:p.Arg126Gln
XM_011521862.3:c.377G>A	XP_011520164.1:p.Arg126Gln