Canonical Allele Identifier: CA7484032

Gene: RAD51

Linked Data

• dbSNP Id: rs748483725
• ExAC: 15:41011117 AAG / A
• gnomAD v2: 15-41011117-AAG-A
• gnomAD v4: 15-40718919-AAG-A
• MyVariant Identifiers: chr15:g.41011118_41011119del (hg19) ; chr15:g.40718920_40718921del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.40718925_40718926del , CM000677.2:g.40718925_40718926del	GRCh38
NC_000015.9:g.41011123_41011124del , CM000677.1:g.41011123_41011124del	GRCh37
NC_000015.8:g.38798415_38798416del	NCBI36
NG_012120.1:g.28765_28766del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000267868.8:c.530+26_530+27del MANE Select	ENSP00000267868.3:n.530+26_530+27del
ENST00000532743.6:c.530+26_530+27del	ENSP00000433924.2:n.530+26_530+27del
ENST00000645673.2:c.533+26_533+27del	ENSP00000493712.2:n.533+26_533+27del
ENST00000267868.7:c.530+26_530+27del	ENSP00000267868.3:n.530+26_530+27del
ENST00000382643.7:c.533+26_533+27del	ENSP00000372088.3:n.533+26_533+27del
ENST00000423169.6:c.530+26_530+27del	ENSP00000406602.2:n.530+26_530+27del
ENST00000525066.5:c.436-9786_436-9785del	ENSP00000431864.1:n.436-9786_436-9785del
ENST00000531277.2:c.*109+26_*109+27del	ENSP00000436512.2:n.*109+26_*109+27del
ENST00000532743.5:c.533+26_533+27del	ENSP00000433924.1:n.533+26_533+27del
ENST00000557850.5:c.239+26_239+27del	ENSP00000454176.1:n.239+26_239+27del
NM_001164269.1:c.533+26_533+27del	NP_001157741.1:n.533+26_533+27del
NM_001164270.1:c.530+26_530+27del	NP_001157742.1:n.530+26_530+27del
NM_002875.4:c.530+26_530+27del	NP_002866.2:n.530+26_530+27del
NM_133487.3:c.533+26_533+27del	NP_597994.3:n.533+26_533+27del
XM_006720626.2:c.530+26_530+27del	XP_006720689.1:n.530+26_530+27del
XM_011521857.1:c.530+26_530+27del	XP_011520159.1:n.530+26_530+27del
XM_011521858.1:c.530+26_530+27del	XP_011520160.1:n.530+26_530+27del
XM_011521859.1:c.530+26_530+27del	XP_011520161.1:n.530+26_530+27del
XM_011521860.1:c.530+26_530+27del	XP_011520162.1:n.530+26_530+27del
XM_011521861.1:c.530+26_530+27del	XP_011520163.1:n.530+26_530+27del
XM_011521862.1:c.158+26_158+27del	XP_011520164.1:n.158+26_158+27del
XM_006720626.3:c.530+26_530+27del	XP_006720689.1:n.530+26_530+27del
XM_011521857.2:c.530+26_530+27del	XP_011520159.1:n.530+26_530+27del
XM_011521858.2:c.530+26_530+27del	XP_011520160.1:n.530+26_530+27del
XM_011521859.2:c.530+26_530+27del	XP_011520161.1:n.530+26_530+27del
XM_011521860.2:c.530+26_530+27del	XP_011520162.1:n.530+26_530+27del
XM_011521861.2:c.530+26_530+27del	XP_011520163.1:n.530+26_530+27del
XM_011521862.3:c.158+26_158+27del	XP_011520164.1:n.158+26_158+27del
NM_001164269.2:c.533+26_533+27del	NP_001157741.1:n.533+26_533+27del
NM_001164270.2:c.530+26_530+27del	NP_001157742.1:n.530+26_530+27del
NM_002875.5:c.530+26_530+27del MANE Select	NP_002866.2:n.530+26_530+27del
NM_133487.4:c.533+26_533+27del	NP_597994.3:n.533+26_533+27del