Canonical Allele Identifier: CA268843912

Gene: RAD51

Linked Data

• dbSNP Id: rs536019921
• gnomAD v3: 15-40718819-G-C
• gnomAD v4: 15-40718819-G-C
• MyVariant Identifiers: chr15:g.41011017G>C (hg19) ; chr15:g.40718819G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.40718819G>C , CM000677.2:g.40718819G>C	GRCh38
NC_000015.9:g.41011017G>C , CM000677.1:g.41011017G>C	GRCh37
NC_000015.8:g.38798309G>C	NCBI36
NG_012120.1:g.28659G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000267868.8:c.450G>C MANE Select	ENSP00000267868.3:p.Arg150=
ENST00000532743.6:c.450G>C	ENSP00000433924.2:p.Arg150=
ENST00000645673.2:c.453G>C	ENSP00000493712.2:p.Arg151=
ENST00000267868.7:c.450G>C	ENSP00000267868.3:p.Arg150=
ENST00000382643.7:c.453G>C	ENSP00000372088.3:p.Arg151=
ENST00000423169.6:c.450G>C	ENSP00000406602.2:p.Arg150=
ENST00000525066.5:c.435+9703G>C	ENSP00000431864.1:n.435+9703G>C
ENST00000527860.5:c.450G>C	ENSP00000432759.1:p.Arg150=
ENST00000531277.2:c.*29G>C	ENSP00000436512.2:n.*29G>C
ENST00000532743.5:c.453G>C	ENSP00000433924.1:p.Arg151=
ENST00000533741.1:c.417G>C
ENST00000557850.5:c.226-67G>C	ENSP00000454176.1:n.226-67G>C
NM_001164269.1:c.453G>C	NP_001157741.1:p.Arg151=
NM_001164270.1:c.450G>C	NP_001157742.1:p.Arg150=
NM_002875.4:c.450G>C	NP_002866.2:p.Arg150=
NM_133487.3:c.453G>C	NP_597994.3:p.Arg151=
XM_006720626.2:c.450G>C	XP_006720689.1:p.Arg150=
XM_011521857.1:c.450G>C	XP_011520159.1:p.Arg150=
XM_011521858.1:c.450G>C	XP_011520160.1:p.Arg150=
XM_011521859.1:c.450G>C	XP_011520161.1:p.Arg150=
XM_011521860.1:c.450G>C	XP_011520162.1:p.Arg150=
XM_011521861.1:c.450G>C	XP_011520163.1:p.Arg150=
XM_011521862.1:c.78G>C	XP_011520164.1:p.Arg26=
XM_006720626.3:c.450G>C	XP_006720689.1:p.Arg150=
XM_011521857.2:c.450G>C	XP_011520159.1:p.Arg150=
XM_011521858.2:c.450G>C	XP_011520160.1:p.Arg150=
XM_011521859.2:c.450G>C	XP_011520161.1:p.Arg150=
XM_011521860.2:c.450G>C	XP_011520162.1:p.Arg150=
XM_011521861.2:c.450G>C	XP_011520163.1:p.Arg150=
XM_011521862.3:c.78G>C	XP_011520164.1:p.Arg26=
NM_001164269.2:c.453G>C	NP_001157741.1:p.Arg151=
NM_001164270.2:c.450G>C	NP_001157742.1:p.Arg150=
NM_002875.5:c.450G>C MANE Select	NP_002866.2:p.Arg150=
NM_133487.4:c.453G>C	NP_597994.3:p.Arg151=