Canonical Allele Identifier: CA2803865392

Gene: RAD51

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.40695325del , CM000677.2:g.40695325del	GRCh38
NC_000015.9:g.40987523del , CM000677.1:g.40987523del	GRCh37
NC_000015.8:g.38774815del	NCBI36
NG_012120.1:g.5165del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000267868.8:c.-103del MANE Select	ENSP00000267868.3:n.-103del
ENST00000645673.2:c.-103del	ENSP00000493712.2:n.-103del
ENST00000267868.7:c.-103del	ENSP00000267868.3:n.-103del
ENST00000382643.7:c.-3+4del	ENSP00000372088.3:n.-3+4del
ENST00000423169.6:c.-103del	ENSP00000406602.2:n.-103del
ENST00000525066.5:c.-103del	ENSP00000431864.1:n.-103del
ENST00000527860.5:c.-3+505del	ENSP00000432759.1:n.-3+505del
ENST00000532743.5:c.-103del	ENSP00000433924.1:n.-103del
ENST00000557850.5:c.-103del	ENSP00000454176.1:n.-103del
NM_001164269.1:c.-3+4del	NP_001157741.1:n.-3+4del
NM_001164270.1:c.-103del	NP_001157742.1:n.-103del
NM_002875.4:c.-103del	NP_002866.2:n.-103del
NM_133487.3:c.-103del	NP_597994.3:n.-103del
XM_011521857.1:c.-3+505del	XP_011520159.1:n.-3+505del
XM_011521860.1:c.-3+4del	XP_011520162.1:n.-3+4del
XM_011521861.1:c.-3+505del	XP_011520163.1:n.-3+505del
XM_011521862.1:c.-357del	XP_011520164.1:n.-357del
XM_011521857.2:c.-3+505del	XP_011520159.1:n.-3+505del
XM_011521860.2:c.-3+4del	XP_011520162.1:n.-3+4del
XM_011521861.2:c.-3+505del	XP_011520163.1:n.-3+505del
XM_011521862.3:c.-357del	XP_011520164.1:n.-357del
NM_001164269.2:c.-3+4del	NP_001157741.1:n.-3+4del
NM_001164270.2:c.-103del	NP_001157742.1:n.-103del
NM_002875.5:c.-103del MANE Select	NP_002866.2:n.-103del
NM_133487.4:c.-103del	NP_597994.3:n.-103del