Canonical Allele Identifier: CA968974938
Gene: RAD51 HGNC NCBI

Linked Data

dbSNP Id: rs1894544881

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.40695340G>T , CM000677.2:g.40695340G>T GRCh38
NC_000015.9:g.40987538G>T , CM000677.1:g.40987538G>T GRCh37
NC_000015.8:g.38774830G>T NCBI36
NG_012120.1:g.5180G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000267868.8:c.-88G>T MANE Select ENSP00000267868.3:n.-88G>T
ENST00000645673.2:c.-88G>T ENSP00000493712.2:n.-88G>T
ENST00000267868.7:c.-88G>T ENSP00000267868.3:n.-88G>T
ENST00000382643.7:c.-3+19G>T ENSP00000372088.3:n.-3+19G>T
ENST00000423169.6:c.-88G>T ENSP00000406602.2:n.-88G>T
ENST00000525066.5:c.-88G>T ENSP00000431864.1:n.-88G>T
ENST00000527860.5:c.-3+520G>T ENSP00000432759.1:n.-3+520G>T
ENST00000532743.5:c.-88G>T ENSP00000433924.1:n.-88G>T
ENST00000557850.5:c.-88G>T ENSP00000454176.1:n.-88G>T
NM_001164269.1:c.-3+19G>T NP_001157741.1:n.-3+19G>T
NM_001164270.1:c.-88G>T NP_001157742.1:n.-88G>T
NM_002875.4:c.-88G>T NP_002866.2:n.-88G>T
NM_133487.3:c.-88G>T NP_597994.3:n.-88G>T
XM_011521857.1:c.-3+520G>T XP_011520159.1:n.-3+520G>T
XM_011521860.1:c.-3+19G>T XP_011520162.1:n.-3+19G>T
XM_011521861.1:c.-3+520G>T XP_011520163.1:n.-3+520G>T
XM_011521862.1:c.-342G>T XP_011520164.1:n.-342G>T
XM_011521857.2:c.-3+520G>T XP_011520159.1:n.-3+520G>T
XM_011521860.2:c.-3+19G>T XP_011520162.1:n.-3+19G>T
XM_011521861.2:c.-3+520G>T XP_011520163.1:n.-3+520G>T
XM_011521862.3:c.-342G>T XP_011520164.1:n.-342G>T
NM_001164269.2:c.-3+19G>T NP_001157741.1:n.-3+19G>T
NM_001164270.2:c.-88G>T NP_001157742.1:n.-88G>T
NM_002875.5:c.-88G>T MANE Select NP_002866.2:n.-88G>T
NM_133487.4:c.-88G>T NP_597994.3:n.-88G>T