Canonical Allele Identifier: CA1950968027

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.8101642_8101647delinsGTTGCC , CM000673.2:g.8101642_8101647delinsGTTGCC GRCh38
NC_000011.9:g.8123189_8123194delinsGTTGCC , CM000673.1:g.8123189_8123194delinsGTTGCC GRCh37
NC_000011.8:g.8079765_8079770delinsGTTGCC NCBI36
NG_029912.1:g.68010_68015delinsGTTGCC
NG_030416.2:g.72397_72402delinsGGCAAC

Transcript Alleles

HGVS Amino-acid Change
ENST00000299506.3:c.*23_*28delinsGTTGCC (TUB) MANE Select ENSP00000299506.3:n.*23_*28delinsGTTGCC
ENST00000299506.2:c.*23_*28delinsGTTGCC (TUB) ENSP00000299506.2:n.*23_*28delinsGTTGCC
ENST00000305253.8:c.*23_*28delinsGTTGCC (TUB) ENSP00000305426.4:n.*23_*28delinsGTTGCC
ENST00000534099.5:c.*23_*28delinsGTTGCC (TUB) ENSP00000434400.1:n.*23_*28delinsGTTGCC
NM_003320.4:c.*23_*28delinsGTTGCC (TUB) NP_003311.2:n.*23_*28delinsGTTGCC
NM_177972.2:c.*23_*28delinsGTTGCC (TUB) NP_813977.1:n.*23_*28delinsGTTGCC
XM_005253109.2:c.*23_*28delinsGTTGCC (TUB) XP_005253166.1:n.*23_*28delinsGTTGCC
XM_011520344.1:c.*23_*28delinsGTTGCC (TUB) XP_011518646.1:n.*23_*28delinsGTTGCC
XR_428851.2:n.1484-7488_1484-7483delinsGGCAAC (RIC3)
XR_930896.1:n.1546+5688_1546+5693delinsGGCAAC (RIC3)
XR_930900.1:n.1547-3925_1547-3920delinsGGCAAC (RIC3)
NR_144485.1:n.1519+5688_1519+5693delinsGGCAAC (RIC3)
XM_005253109.3:c.*23_*28delinsGTTGCC (TUB) XP_005253166.1:n.*23_*28delinsGTTGCC
XM_011520344.2:c.*23_*28delinsGTTGCC (TUB) XP_011518646.1:n.*23_*28delinsGTTGCC
XR_001747957.2:n.1335-7488_1335-7483delinsGGCAAC (RIC3)
XR_428851.4:n.1422-7488_1422-7483delinsGGCAAC (RIC3)
XR_930896.3:n.1484+5688_1484+5693delinsGGCAAC (RIC3)
XR_930900.3:n.1485-3925_1485-3920delinsGGCAAC (RIC3)
NM_177972.3:c.*23_*28delinsGTTGCC (TUB) MANE Select NP_813977.1:n.*23_*28delinsGTTGCC
NR_144485.2:n.1450+5688_1450+5693delinsGGCAAC (RIC3)
NM_003320.5:c.*23_*28delinsGTTGCC (TUB) NP_003311.2:n.*23_*28delinsGTTGCC