Canonical Allele Identifier: CA391753680
Gene: RAD51 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.40718893C>G , CM000677.2:g.40718893C>G GRCh38
NC_000015.9:g.41011091C>G , CM000677.1:g.41011091C>G GRCh37
NC_000015.8:g.38798383C>G NCBI36
NG_012120.1:g.28733C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000267868.8:c.524C>G MANE Select ENSP00000267868.3:p.Ala175Gly
ENST00000532743.6:c.524C>G ENSP00000433924.2:p.Ala175Gly
ENST00000645673.2:c.527C>G ENSP00000493712.2:p.Ala176Gly
ENST00000267868.7:c.524C>G ENSP00000267868.3:p.Ala175Gly
ENST00000382643.7:c.527C>G ENSP00000372088.3:p.Ala176Gly
ENST00000423169.6:c.524C>G ENSP00000406602.2:p.Ala175Gly
ENST00000525066.5:c.435+9777C>G ENSP00000431864.1:n.435+9777C>G
ENST00000531277.2:c.*103C>G ENSP00000436512.2:n.*103C>G
ENST00000532743.5:c.527C>G ENSP00000433924.1:p.Ala176Gly
ENST00000557850.5:c.233C>G ENSP00000454176.1:p.Ala78Gly
NM_001164269.1:c.527C>G NP_001157741.1:p.Ala176Gly
NM_001164270.1:c.524C>G NP_001157742.1:p.Ala175Gly
NM_002875.4:c.524C>G NP_002866.2:p.Ala175Gly
NM_133487.3:c.527C>G NP_597994.3:p.Ala176Gly
XM_006720626.2:c.524C>G XP_006720689.1:p.Ala175Gly
XM_011521857.1:c.524C>G XP_011520159.1:p.Ala175Gly
XM_011521858.1:c.524C>G XP_011520160.1:p.Ala175Gly
XM_011521859.1:c.524C>G XP_011520161.1:p.Ala175Gly
XM_011521860.1:c.524C>G XP_011520162.1:p.Ala175Gly
XM_011521861.1:c.524C>G XP_011520163.1:p.Ala175Gly
XM_011521862.1:c.152C>G XP_011520164.1:p.Ala51Gly
XM_006720626.3:c.524C>G XP_006720689.1:p.Ala175Gly
XM_011521857.2:c.524C>G XP_011520159.1:p.Ala175Gly
XM_011521858.2:c.524C>G XP_011520160.1:p.Ala175Gly
XM_011521859.2:c.524C>G XP_011520161.1:p.Ala175Gly
XM_011521860.2:c.524C>G XP_011520162.1:p.Ala175Gly
XM_011521861.2:c.524C>G XP_011520163.1:p.Ala175Gly
XM_011521862.3:c.152C>G XP_011520164.1:p.Ala51Gly
NM_001164269.2:c.527C>G NP_001157741.1:p.Ala176Gly
NM_001164270.2:c.524C>G NP_001157742.1:p.Ala175Gly
NM_002875.5:c.524C>G MANE Select NP_002866.2:p.Ala175Gly
NM_133487.4:c.527C>G NP_597994.3:p.Ala176Gly