Canonical Allele Identifier: CA391753230

Gene: RAD51

Linked Data

• ClinVar Variation Id: 1740273
• ClinVar RCV Id: RCV002333692
• MyVariant Identifiers: chr15:g.41011006C>A (hg19) ; chr15:g.40718808C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.40718808C>A , CM000677.2:g.40718808C>A	GRCh38
NC_000015.9:g.41011006C>A , CM000677.1:g.41011006C>A	GRCh37
NC_000015.8:g.38798298C>A	NCBI36
NG_012120.1:g.28648C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000267868.8:c.439C>A MANE Select	ENSP00000267868.3:p.Pro147Thr
ENST00000532743.6:c.439C>A	ENSP00000433924.2:p.Pro147Thr
ENST00000645673.2:c.442C>A	ENSP00000493712.2:p.Pro148Thr
ENST00000267868.7:c.439C>A	ENSP00000267868.3:p.Pro147Thr
ENST00000382643.7:c.442C>A	ENSP00000372088.3:p.Pro148Thr
ENST00000423169.6:c.439C>A	ENSP00000406602.2:p.Pro147Thr
ENST00000525066.5:c.435+9692C>A	ENSP00000431864.1:n.435+9692C>A
ENST00000527860.5:c.439C>A	ENSP00000432759.1:p.Pro147Thr
ENST00000531277.2:c.*18C>A	ENSP00000436512.2:n.*18C>A
ENST00000532743.5:c.442C>A	ENSP00000433924.1:p.Pro148Thr
ENST00000533741.1:c.406C>A
ENST00000557850.5:c.226-78C>A	ENSP00000454176.1:n.226-78C>A
NM_001164269.1:c.442C>A	NP_001157741.1:p.Pro148Thr
NM_001164270.1:c.439C>A	NP_001157742.1:p.Pro147Thr
NM_002875.4:c.439C>A	NP_002866.2:p.Pro147Thr
NM_133487.3:c.442C>A	NP_597994.3:p.Pro148Thr
XM_006720626.2:c.439C>A	XP_006720689.1:p.Pro147Thr
XM_011521857.1:c.439C>A	XP_011520159.1:p.Pro147Thr
XM_011521858.1:c.439C>A	XP_011520160.1:p.Pro147Thr
XM_011521859.1:c.439C>A	XP_011520161.1:p.Pro147Thr
XM_011521860.1:c.439C>A	XP_011520162.1:p.Pro147Thr
XM_011521861.1:c.439C>A	XP_011520163.1:p.Pro147Thr
XM_011521862.1:c.67C>A	XP_011520164.1:p.Pro23Thr
XM_006720626.3:c.439C>A	XP_006720689.1:p.Pro147Thr
XM_011521857.2:c.439C>A	XP_011520159.1:p.Pro147Thr
XM_011521858.2:c.439C>A	XP_011520160.1:p.Pro147Thr
XM_011521859.2:c.439C>A	XP_011520161.1:p.Pro147Thr
XM_011521860.2:c.439C>A	XP_011520162.1:p.Pro147Thr
XM_011521861.2:c.439C>A	XP_011520163.1:p.Pro147Thr
XM_011521862.3:c.67C>A	XP_011520164.1:p.Pro23Thr
NM_001164269.2:c.442C>A	NP_001157741.1:p.Pro148Thr
NM_001164270.2:c.439C>A	NP_001157742.1:p.Pro147Thr
NM_002875.5:c.439C>A MANE Select	NP_002866.2:p.Pro147Thr
NM_133487.4:c.442C>A	NP_597994.3:p.Pro148Thr