Canonical Allele Identifier: CA968974942
Gene: RAD51 HGNC NCBI

Linked Data

dbSNP Id: rs1894545292

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.40695343C>T , CM000677.2:g.40695343C>T GRCh38
NC_000015.9:g.40987541C>T , CM000677.1:g.40987541C>T GRCh37
NC_000015.8:g.38774833C>T NCBI36
NG_012120.1:g.5183C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000267868.8:c.-85C>T MANE Select ENSP00000267868.3:n.-85C>T
ENST00000645673.2:c.-85C>T ENSP00000493712.2:n.-85C>T
ENST00000267868.7:c.-85C>T ENSP00000267868.3:n.-85C>T
ENST00000382643.7:c.-3+22C>T ENSP00000372088.3:n.-3+22C>T
ENST00000423169.6:c.-85C>T ENSP00000406602.2:n.-85C>T
ENST00000525066.5:c.-85C>T ENSP00000431864.1:n.-85C>T
ENST00000527860.5:c.-3+523C>T ENSP00000432759.1:n.-3+523C>T
ENST00000532743.5:c.-85C>T ENSP00000433924.1:n.-85C>T
ENST00000557850.5:c.-85C>T ENSP00000454176.1:n.-85C>T
NM_001164269.1:c.-3+22C>T NP_001157741.1:n.-3+22C>T
NM_001164270.1:c.-85C>T NP_001157742.1:n.-85C>T
NM_002875.4:c.-85C>T NP_002866.2:n.-85C>T
NM_133487.3:c.-85C>T NP_597994.3:n.-85C>T
XM_011521857.1:c.-3+523C>T XP_011520159.1:n.-3+523C>T
XM_011521860.1:c.-3+22C>T XP_011520162.1:n.-3+22C>T
XM_011521861.1:c.-3+523C>T XP_011520163.1:n.-3+523C>T
XM_011521862.1:c.-339C>T XP_011520164.1:n.-339C>T
XM_011521857.2:c.-3+523C>T XP_011520159.1:n.-3+523C>T
XM_011521860.2:c.-3+22C>T XP_011520162.1:n.-3+22C>T
XM_011521861.2:c.-3+523C>T XP_011520163.1:n.-3+523C>T
XM_011521862.3:c.-339C>T XP_011520164.1:n.-339C>T
NM_001164269.2:c.-3+22C>T NP_001157741.1:n.-3+22C>T
NM_001164270.2:c.-85C>T NP_001157742.1:n.-85C>T
NM_002875.5:c.-85C>T MANE Select NP_002866.2:n.-85C>T
NM_133487.4:c.-85C>T NP_597994.3:n.-85C>T