Canonical Allele Identifier: CA2171900100

Gene: RAD51

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.40695337T= , CM000677.2:g.40695337T=	GRCh38
NC_000015.9:g.40987535T= , CM000677.1:g.40987535T=	GRCh37
NC_000015.8:g.38774827T=	NCBI36
NG_012120.1:g.5177T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000267868.8:c.-91T= MANE Select	ENSP00000267868.3:n.-91T=
ENST00000645673.2:c.-91T=	ENSP00000493712.2:n.-91T=
ENST00000267868.7:c.-91T=	ENSP00000267868.3:n.-91T=
ENST00000382643.7:c.-3+16T=	ENSP00000372088.3:n.-3+16T=
ENST00000423169.6:c.-91T=	ENSP00000406602.2:n.-91T=
ENST00000525066.5:c.-91T=	ENSP00000431864.1:n.-91T=
ENST00000527860.5:c.-3+517T=	ENSP00000432759.1:n.-3+517T=
ENST00000532743.5:c.-91T=	ENSP00000433924.1:n.-91T=
ENST00000557850.5:c.-91T=	ENSP00000454176.1:n.-91T=
NM_001164269.1:c.-3+16T=	NP_001157741.1:n.-3+16T=
NM_001164270.1:c.-91T=	NP_001157742.1:n.-91T=
NM_002875.4:c.-91T=	NP_002866.2:n.-91T=
NM_133487.3:c.-91T=	NP_597994.3:n.-91T=
XM_011521857.1:c.-3+517T=	XP_011520159.1:n.-3+517T=
XM_011521860.1:c.-3+16T=	XP_011520162.1:n.-3+16T=
XM_011521861.1:c.-3+517T=	XP_011520163.1:n.-3+517T=
XM_011521862.1:c.-345T=	XP_011520164.1:n.-345T=
XM_011521857.2:c.-3+517T=	XP_011520159.1:n.-3+517T=
XM_011521860.2:c.-3+16T=	XP_011520162.1:n.-3+16T=
XM_011521861.2:c.-3+517T=	XP_011520163.1:n.-3+517T=
XM_011521862.3:c.-345T=	XP_011520164.1:n.-345T=
NM_001164269.2:c.-3+16T=	NP_001157741.1:n.-3+16T=
NM_001164270.2:c.-91T=	NP_001157742.1:n.-91T=
NM_002875.5:c.-91T= MANE Select	NP_002866.2:n.-91T=
NM_133487.4:c.-91T=	NP_597994.3:n.-91T=