Canonical Allele Identifier: CA2790353755

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.8101856_8101857insTTATGGCGTG , CM000673.2:g.8101856_8101857insTTATGGCGTG GRCh38
NC_000011.9:g.8123403_8123404insTTATGGCGTG , CM000673.1:g.8123403_8123404insTTATGGCGTG GRCh37
NC_000011.8:g.8079979_8079980insTTATGGCGTG NCBI36
NG_029912.1:g.68224_68225insTTATGGCGTG
NG_030416.2:g.72189_72190insCGCCATAACA

Transcript Alleles

HGVS Amino-acid Change
ENST00000299506.3:c.*237_*238insTTATGGCGTG (TUB) MANE Select ENSP00000299506.3:n.*237_*238insTTATGGCGTG
ENST00000299506.2:c.*237_*238insTTATGGCGTG (TUB) ENSP00000299506.2:n.*237_*238insTTATGGCGTG
ENST00000305253.8:c.*237_*238insTTATGGCGTG (TUB) ENSP00000305426.4:n.*237_*238insTTATGGCGTG
NM_003320.4:c.*237_*238insTTATGGCGTG (TUB) NP_003311.2:n.*237_*238insTTATGGCGTG
NM_177972.2:c.*237_*238insTTATGGCGTG (TUB) NP_813977.1:n.*237_*238insTTATGGCGTG
XM_005253109.2:c.*237_*238insTTATGGCGTG (TUB) XP_005253166.1:n.*237_*238insTTATGGCGTG
XM_011520344.1:c.*237_*238insTTATGGCGTG (TUB) XP_011518646.1:n.*237_*238insTTATGGCGTG
XR_428851.2:n.1484-7696_1484-7695insCGCCATAACA (RIC3)
XR_930896.1:n.1546+5480_1546+5481insCGCCATAACA (RIC3)
XR_930900.1:n.1547-4133_1547-4132insCGCCATAACA (RIC3)
NR_144485.1:n.1519+5480_1519+5481insCGCCATAACA (RIC3)
XM_005253109.3:c.*237_*238insTTATGGCGTG (TUB) XP_005253166.1:n.*237_*238insTTATGGCGTG
XM_011520344.2:c.*237_*238insTTATGGCGTG (TUB) XP_011518646.1:n.*237_*238insTTATGGCGTG
XR_001747957.2:n.1335-7696_1335-7695insCGCCATAACA (RIC3)
XR_428851.4:n.1422-7696_1422-7695insCGCCATAACA (RIC3)
XR_930896.3:n.1484+5480_1484+5481insCGCCATAACA (RIC3)
XR_930900.3:n.1485-4133_1485-4132insCGCCATAACA (RIC3)
NM_177972.3:c.*237_*238insTTATGGCGTG (TUB) MANE Select NP_813977.1:n.*237_*238insTTATGGCGTG
NR_144485.2:n.1450+5480_1450+5481insCGCCATAACA (RIC3)
NM_003320.5:c.*237_*238insTTATGGCGTG (TUB) NP_003311.2:n.*237_*238insTTATGGCGTG