Canonical Allele Identifier: CA2171911649

Gene: RAD51

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.40718807T= , CM000677.2:g.40718807T=	GRCh38
NC_000015.9:g.41011005T= , CM000677.1:g.41011005T=	GRCh37
NC_000015.8:g.38798297T=	NCBI36
NG_012120.1:g.28647T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000267868.8:c.438T= MANE Select	ENSP00000267868.3:p.Leu146=
ENST00000532743.6:c.438T=	ENSP00000433924.2:p.Leu146=
ENST00000645673.2:c.441T=	ENSP00000493712.2:p.Leu147=
ENST00000267868.7:c.438T=	ENSP00000267868.3:p.Leu146=
ENST00000382643.7:c.441T=	ENSP00000372088.3:p.Leu147=
ENST00000423169.6:c.438T=	ENSP00000406602.2:p.Leu146=
ENST00000525066.5:c.435+9691T=	ENSP00000431864.1:n.435+9691T=
ENST00000527860.5:c.438T=	ENSP00000432759.1:p.Leu146=
ENST00000531277.2:c.*17T=	ENSP00000436512.2:n.*17T=
ENST00000532743.5:c.441T=	ENSP00000433924.1:p.Leu147=
ENST00000533741.1:c.405T=
ENST00000557850.5:c.226-79T=	ENSP00000454176.1:n.226-79T=
NM_001164269.1:c.441T=	NP_001157741.1:p.Leu147=
NM_001164270.1:c.438T=	NP_001157742.1:p.Leu146=
NM_002875.4:c.438T=	NP_002866.2:p.Leu146=
NM_133487.3:c.441T=	NP_597994.3:p.Leu147=
XM_006720626.2:c.438T=	XP_006720689.1:p.Leu146=
XM_011521857.1:c.438T=	XP_011520159.1:p.Leu146=
XM_011521858.1:c.438T=	XP_011520160.1:p.Leu146=
XM_011521859.1:c.438T=	XP_011520161.1:p.Leu146=
XM_011521860.1:c.438T=	XP_011520162.1:p.Leu146=
XM_011521861.1:c.438T=	XP_011520163.1:p.Leu146=
XM_011521862.1:c.66T=	XP_011520164.1:p.Leu22=
XM_006720626.3:c.438T=	XP_006720689.1:p.Leu146=
XM_011521857.2:c.438T=	XP_011520159.1:p.Leu146=
XM_011521858.2:c.438T=	XP_011520160.1:p.Leu146=
XM_011521859.2:c.438T=	XP_011520161.1:p.Leu146=
XM_011521860.2:c.438T=	XP_011520162.1:p.Leu146=
XM_011521861.2:c.438T=	XP_011520163.1:p.Leu146=
XM_011521862.3:c.66T=	XP_011520164.1:p.Leu22=
NM_001164269.2:c.441T=	NP_001157741.1:p.Leu147=
NM_001164270.2:c.438T=	NP_001157742.1:p.Leu146=
NM_002875.5:c.438T= MANE Select	NP_002866.2:p.Leu146=
NM_133487.4:c.441T=	NP_597994.3:p.Leu147=