Canonical Allele Identifier: CA489772865

Gene: RAD51

Linked Data

• gnomAD v4: 15-40718810-C-A
• MyVariant Identifiers: chr15:g.41011008C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.40718810C>A , CM000677.2:g.40718810C>A	GRCh38
NC_000015.9:g.41011008C>A , CM000677.1:g.41011008C>A	GRCh37
NC_000015.8:g.38798300C>A	NCBI36
NG_012120.1:g.28650C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000267868.8:c.441C>A MANE Select	ENSP00000267868.3:p.Pro147=
ENST00000532743.6:c.441C>A	ENSP00000433924.2:p.Pro147=
ENST00000645673.2:c.444C>A	ENSP00000493712.2:p.Pro148=
ENST00000267868.7:c.441C>A	ENSP00000267868.3:p.Pro147=
ENST00000382643.7:c.444C>A	ENSP00000372088.3:p.Pro148=
ENST00000423169.6:c.441C>A	ENSP00000406602.2:p.Pro147=
ENST00000525066.5:c.435+9694C>A	ENSP00000431864.1:n.435+9694C>A
ENST00000527860.5:c.441C>A	ENSP00000432759.1:p.Pro147=
ENST00000531277.2:c.*20C>A	ENSP00000436512.2:n.*20C>A
ENST00000532743.5:c.444C>A	ENSP00000433924.1:p.Pro148=
ENST00000533741.1:c.408C>A
ENST00000557850.5:c.226-76C>A	ENSP00000454176.1:n.226-76C>A
NM_001164269.1:c.444C>A	NP_001157741.1:p.Pro148=
NM_001164270.1:c.441C>A	NP_001157742.1:p.Pro147=
NM_002875.4:c.441C>A	NP_002866.2:p.Pro147=
NM_133487.3:c.444C>A	NP_597994.3:p.Pro148=
XM_006720626.2:c.441C>A	XP_006720689.1:p.Pro147=
XM_011521857.1:c.441C>A	XP_011520159.1:p.Pro147=
XM_011521858.1:c.441C>A	XP_011520160.1:p.Pro147=
XM_011521859.1:c.441C>A	XP_011520161.1:p.Pro147=
XM_011521860.1:c.441C>A	XP_011520162.1:p.Pro147=
XM_011521861.1:c.441C>A	XP_011520163.1:p.Pro147=
XM_011521862.1:c.69C>A	XP_011520164.1:p.Pro23=
XM_006720626.3:c.441C>A	XP_006720689.1:p.Pro147=
XM_011521857.2:c.441C>A	XP_011520159.1:p.Pro147=
XM_011521858.2:c.441C>A	XP_011520160.1:p.Pro147=
XM_011521859.2:c.441C>A	XP_011520161.1:p.Pro147=
XM_011521860.2:c.441C>A	XP_011520162.1:p.Pro147=
XM_011521861.2:c.441C>A	XP_011520163.1:p.Pro147=
XM_011521862.3:c.69C>A	XP_011520164.1:p.Pro23=
NM_001164269.2:c.444C>A	NP_001157741.1:p.Pro148=
NM_001164270.2:c.441C>A	NP_001157742.1:p.Pro147=
NM_002875.5:c.441C>A MANE Select	NP_002866.2:p.Pro147=
NM_133487.4:c.444C>A	NP_597994.3:p.Pro148=