Canonical Allele Identifier: CA2612334416

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.8101854_8101855insG , CM000673.2:g.8101854_8101855insG GRCh38
NC_000011.9:g.8123401_8123402insG , CM000673.1:g.8123401_8123402insG GRCh37
NC_000011.8:g.8079977_8079978insG NCBI36
NG_029912.1:g.68222_68223insG
NG_030416.2:g.72189_72190insC

Transcript Alleles

HGVS Amino-acid Change
ENST00000299506.3:c.*235_*236insG (TUB) MANE Select ENSP00000299506.3:n.*235_*236insG
ENST00000299506.2:c.*235_*236insG (TUB) ENSP00000299506.2:n.*235_*236insG
ENST00000305253.8:c.*235_*236insG (TUB) ENSP00000305426.4:n.*235_*236insG
NM_003320.4:c.*235_*236insG (TUB) NP_003311.2:n.*235_*236insG
NM_177972.2:c.*235_*236insG (TUB) NP_813977.1:n.*235_*236insG
XM_005253109.2:c.*235_*236insG (TUB) XP_005253166.1:n.*235_*236insG
XM_011520344.1:c.*235_*236insG (TUB) XP_011518646.1:n.*235_*236insG
XR_428851.2:n.1484-7696_1484-7695insC (RIC3)
XR_930896.1:n.1546+5480_1546+5481insC (RIC3)
XR_930900.1:n.1547-4133_1547-4132insC (RIC3)
NR_144485.1:n.1519+5480_1519+5481insC (RIC3)
XM_005253109.3:c.*235_*236insG (TUB) XP_005253166.1:n.*235_*236insG
XM_011520344.2:c.*235_*236insG (TUB) XP_011518646.1:n.*235_*236insG
XR_001747957.2:n.1335-7696_1335-7695insC (RIC3)
XR_428851.4:n.1422-7696_1422-7695insC (RIC3)
XR_930896.3:n.1484+5480_1484+5481insC (RIC3)
XR_930900.3:n.1485-4133_1485-4132insC (RIC3)
NM_177972.3:c.*235_*236insG (TUB) MANE Select NP_813977.1:n.*235_*236insG
NR_144485.2:n.1450+5480_1450+5481insC (RIC3)
NM_003320.5:c.*235_*236insG (TUB) NP_003311.2:n.*235_*236insG