Canonical Allele Identifier: CA391753588

Gene: RAD51

Linked Data

• dbSNP Id: rs2141857547
• gnomAD v4: 15-40718877-C-T
• MyVariant Identifiers: chr15:g.41011075C>T (hg19) ; chr15:g.40718877C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.40718877C>T , CM000677.2:g.40718877C>T	GRCh38
NC_000015.9:g.41011075C>T , CM000677.1:g.41011075C>T	GRCh37
NC_000015.8:g.38798367C>T	NCBI36
NG_012120.1:g.28717C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000267868.8:c.508C>T MANE Select	ENSP00000267868.3:p.Arg170Trp
ENST00000532743.6:c.508C>T	ENSP00000433924.2:p.Arg170Trp
ENST00000645673.2:c.511C>T	ENSP00000493712.2:p.Arg171Trp
ENST00000267868.7:c.508C>T	ENSP00000267868.3:p.Arg170Trp
ENST00000382643.7:c.511C>T	ENSP00000372088.3:p.Arg171Trp
ENST00000423169.6:c.508C>T	ENSP00000406602.2:p.Arg170Trp
ENST00000525066.5:c.435+9761C>T	ENSP00000431864.1:n.435+9761C>T
ENST00000527860.5:c.508C>T	ENSP00000432759.1:p.Arg170Trp
ENST00000531277.2:c.*87C>T	ENSP00000436512.2:n.*87C>T
ENST00000532743.5:c.511C>T	ENSP00000433924.1:p.Arg171Trp
ENST00000557850.5:c.226-9C>T	ENSP00000454176.1:n.226-9C>T
NM_001164269.1:c.511C>T	NP_001157741.1:p.Arg171Trp
NM_001164270.1:c.508C>T	NP_001157742.1:p.Arg170Trp
NM_002875.4:c.508C>T	NP_002866.2:p.Arg170Trp
NM_133487.3:c.511C>T	NP_597994.3:p.Arg171Trp
XM_006720626.2:c.508C>T	XP_006720689.1:p.Arg170Trp
XM_011521857.1:c.508C>T	XP_011520159.1:p.Arg170Trp
XM_011521858.1:c.508C>T	XP_011520160.1:p.Arg170Trp
XM_011521859.1:c.508C>T	XP_011520161.1:p.Arg170Trp
XM_011521860.1:c.508C>T	XP_011520162.1:p.Arg170Trp
XM_011521861.1:c.508C>T	XP_011520163.1:p.Arg170Trp
XM_011521862.1:c.136C>T	XP_011520164.1:p.Arg46Trp
XM_006720626.3:c.508C>T	XP_006720689.1:p.Arg170Trp
XM_011521857.2:c.508C>T	XP_011520159.1:p.Arg170Trp
XM_011521858.2:c.508C>T	XP_011520160.1:p.Arg170Trp
XM_011521859.2:c.508C>T	XP_011520161.1:p.Arg170Trp
XM_011521860.2:c.508C>T	XP_011520162.1:p.Arg170Trp
XM_011521861.2:c.508C>T	XP_011520163.1:p.Arg170Trp
XM_011521862.3:c.136C>T	XP_011520164.1:p.Arg46Trp
NM_001164269.2:c.511C>T	NP_001157741.1:p.Arg171Trp
NM_001164270.2:c.508C>T	NP_001157742.1:p.Arg170Trp
NM_002875.5:c.508C>T MANE Select	NP_002866.2:p.Arg170Trp
NM_133487.4:c.511C>T	NP_597994.3:p.Arg171Trp