Canonical Allele Identifier: CA268836784
Gene: RAD51 HGNC NCBI

Linked Data

dbSNP Id: rs1036800475

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.40695377_40695394del , CM000677.2:g.40695377_40695394del GRCh38
NC_000015.9:g.40987575_40987592del , CM000677.1:g.40987575_40987592del GRCh37
NC_000015.8:g.38774867_38774884del NCBI36
NG_012120.1:g.5217_5234del

Transcript Alleles

HGVS Amino-acid Change
ENST00000267868.8:c.-51_-34del MANE Select ENSP00000267868.3:n.-51_-34del
ENST00000645673.2:c.-51_-34del ENSP00000493712.2:n.-51_-34del
ENST00000267868.7:c.-51_-34del ENSP00000267868.3:n.-51_-34del
ENST00000382643.7:c.-3+56_-3+73del ENSP00000372088.3:n.-3+56_-3+73del
ENST00000423169.6:c.-51_-34del ENSP00000406602.2:n.-51_-34del
ENST00000525066.5:c.-51_-34del ENSP00000431864.1:n.-51_-34del
ENST00000527860.5:c.-3+557_-3+574del ENSP00000432759.1:n.-3+557_-3+574del
ENST00000532743.5:c.-51_-34del ENSP00000433924.1:n.-51_-34del
ENST00000557850.5:c.-51_-34del ENSP00000454176.1:n.-51_-34del
NM_001164269.1:c.-3+56_-3+73del NP_001157741.1:n.-3+56_-3+73del
NM_001164270.1:c.-51_-34del NP_001157742.1:n.-51_-34del
NM_002875.4:c.-51_-34del NP_002866.2:n.-51_-34del
NM_133487.3:c.-51_-34del NP_597994.3:n.-51_-34del
XM_011521857.1:c.-3+557_-3+574del XP_011520159.1:n.-3+557_-3+574del
XM_011521860.1:c.-3+56_-3+73del XP_011520162.1:n.-3+56_-3+73del
XM_011521861.1:c.-3+557_-3+574del XP_011520163.1:n.-3+557_-3+574del
XM_011521862.1:c.-305_-288del XP_011520164.1:n.-305_-288del
XM_011521857.2:c.-3+557_-3+574del XP_011520159.1:n.-3+557_-3+574del
XM_011521860.2:c.-3+56_-3+73del XP_011520162.1:n.-3+56_-3+73del
XM_011521861.2:c.-3+557_-3+574del XP_011520163.1:n.-3+557_-3+574del
XM_011521862.3:c.-305_-288del XP_011520164.1:n.-305_-288del
NM_001164269.2:c.-3+56_-3+73del NP_001157741.1:n.-3+56_-3+73del
NM_001164270.2:c.-51_-34del NP_001157742.1:n.-51_-34del
NM_002875.5:c.-51_-34del MANE Select NP_002866.2:n.-51_-34del
NM_133487.4:c.-51_-34del NP_597994.3:n.-51_-34del