Canonical Allele Identifier: CA16044167

Gene: RAD51

Linked Data

• ClinVar Variation Id: 372139
• ClinVar RCV Id: RCV000412566 ; RCV000622620 ; RCV001194792 ; RCV001731668
• dbSNP Id: rs1057519413
• MyVariant Identifiers: chr15:g.41022153G>A (hg19) ; chr15:g.40729955G>A (hg38)
• PubMed: PMID:24808016 ; PMID:25813273 ; PMID:26253028 ; PMID:26681308

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.40729955G>A , CM000677.2:g.40729955G>A	GRCh38
NC_000015.9:g.41022153G>A , CM000677.1:g.41022153G>A	GRCh37
NC_000015.8:g.38809445G>A	NCBI36
NG_012120.1:g.39795G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000267868.8:c.877G>A MANE Select	ENSP00000267868.3:p.Ala293Thr
ENST00000532743.6:c.877G>A	ENSP00000433924.2:p.Ala293Thr
ENST00000645673.2:c.880G>A	ENSP00000493712.2:p.Ala294Thr
ENST00000267868.7:c.877G>A	ENSP00000267868.3:p.Ala293Thr
ENST00000382643.7:c.880G>A	ENSP00000372088.3:p.Ala294Thr
ENST00000423169.6:c.774+321G>A	ENSP00000406602.2:n.774+321G>A
ENST00000525066.5:c.*326G>A	ENSP00000431864.1:n.*326G>A
ENST00000532743.5:c.880G>A	ENSP00000433924.1:p.Ala294Thr
ENST00000557850.5:c.586G>A	ENSP00000454176.1:p.Ala196Thr
NM_001164269.1:c.880G>A	NP_001157741.1:p.Ala294Thr
NM_001164270.1:c.774+321G>A	NP_001157742.1:n.774+321G>A
NM_002875.4:c.877G>A	NP_002866.2:p.Ala293Thr
NM_133487.3:c.880G>A	NP_597994.3:p.Ala294Thr
XM_006720626.2:c.877G>A	XP_006720689.1:p.Ala293Thr
XM_011521857.1:c.877G>A	XP_011520159.1:p.Ala293Thr
XM_011521858.1:c.877G>A	XP_011520160.1:p.Ala293Thr
XM_011521859.1:c.877G>A	XP_011520161.1:p.Ala293Thr
XM_011521860.1:c.877G>A	XP_011520162.1:p.Ala293Thr
XM_011521861.1:c.774+321G>A	XP_011520163.1:n.774+321G>A
XM_011521862.1:c.505G>A	XP_011520164.1:p.Ala169Thr
XM_006720626.3:c.877G>A	XP_006720689.1:p.Ala293Thr
XM_011521857.2:c.877G>A	XP_011520159.1:p.Ala293Thr
XM_011521858.2:c.877G>A	XP_011520160.1:p.Ala293Thr
XM_011521859.2:c.877G>A	XP_011520161.1:p.Ala293Thr
XM_011521860.2:c.877G>A	XP_011520162.1:p.Ala293Thr
XM_011521861.2:c.774+321G>A	XP_011520163.1:n.774+321G>A
XM_011521862.3:c.505G>A	XP_011520164.1:p.Ala169Thr
NM_001164269.2:c.880G>A	NP_001157741.1:p.Ala294Thr
NM_001164270.2:c.774+321G>A	NP_001157742.1:n.774+321G>A
NM_002875.5:c.877G>A MANE Select	NP_002866.2:p.Ala293Thr
NM_133487.4:c.880G>A	NP_597994.3:p.Ala294Thr