Canonical Allele Identifier: CA391753443

Gene: RAD51

Linked Data

• ClinVar Variation Id: 1743549
• ClinVar RCV Id: RCV002330800
• MyVariant Identifiers: chr15:g.41011051A>G (hg19) ; chr15:g.40718853A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.40718853A>G , CM000677.2:g.40718853A>G	GRCh38
NC_000015.9:g.41011051A>G , CM000677.1:g.41011051A>G	GRCh37
NC_000015.8:g.38798343A>G	NCBI36
NG_012120.1:g.28693A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000267868.8:c.484A>G MANE Select	ENSP00000267868.3:p.Thr162Ala
ENST00000532743.6:c.484A>G	ENSP00000433924.2:p.Thr162Ala
ENST00000645673.2:c.487A>G	ENSP00000493712.2:p.Thr163Ala
ENST00000267868.7:c.484A>G	ENSP00000267868.3:p.Thr162Ala
ENST00000382643.7:c.487A>G	ENSP00000372088.3:p.Thr163Ala
ENST00000423169.6:c.484A>G	ENSP00000406602.2:p.Thr162Ala
ENST00000525066.5:c.435+9737A>G	ENSP00000431864.1:n.435+9737A>G
ENST00000527860.5:c.484A>G	ENSP00000432759.1:p.Thr162Ala
ENST00000531277.2:c.*63A>G	ENSP00000436512.2:n.*63A>G
ENST00000532743.5:c.487A>G	ENSP00000433924.1:p.Thr163Ala
ENST00000557850.5:c.226-33A>G	ENSP00000454176.1:n.226-33A>G
NM_001164269.1:c.487A>G	NP_001157741.1:p.Thr163Ala
NM_001164270.1:c.484A>G	NP_001157742.1:p.Thr162Ala
NM_002875.4:c.484A>G	NP_002866.2:p.Thr162Ala
NM_133487.3:c.487A>G	NP_597994.3:p.Thr163Ala
XM_006720626.2:c.484A>G	XP_006720689.1:p.Thr162Ala
XM_011521857.1:c.484A>G	XP_011520159.1:p.Thr162Ala
XM_011521858.1:c.484A>G	XP_011520160.1:p.Thr162Ala
XM_011521859.1:c.484A>G	XP_011520161.1:p.Thr162Ala
XM_011521860.1:c.484A>G	XP_011520162.1:p.Thr162Ala
XM_011521861.1:c.484A>G	XP_011520163.1:p.Thr162Ala
XM_011521862.1:c.112A>G	XP_011520164.1:p.Thr38Ala
XM_006720626.3:c.484A>G	XP_006720689.1:p.Thr162Ala
XM_011521857.2:c.484A>G	XP_011520159.1:p.Thr162Ala
XM_011521858.2:c.484A>G	XP_011520160.1:p.Thr162Ala
XM_011521859.2:c.484A>G	XP_011520161.1:p.Thr162Ala
XM_011521860.2:c.484A>G	XP_011520162.1:p.Thr162Ala
XM_011521861.2:c.484A>G	XP_011520163.1:p.Thr162Ala
XM_011521862.3:c.112A>G	XP_011520164.1:p.Thr38Ala
NM_001164269.2:c.487A>G	NP_001157741.1:p.Thr163Ala
NM_001164270.2:c.484A>G	NP_001157742.1:p.Thr162Ala
NM_002875.5:c.484A>G MANE Select	NP_002866.2:p.Thr162Ala
NM_133487.4:c.487A>G	NP_597994.3:p.Thr163Ala