Canonical Allele Identifier: CA2790351867
Gene: TUB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.8089874_8089876del , CM000673.2:g.8089874_8089876del GRCh38
NC_000011.9:g.8111421_8111423del , CM000673.1:g.8111421_8111423del GRCh37
NC_000011.8:g.8067997_8067999del NCBI36
NG_029912.1:g.56242_56244del

Transcript Alleles

HGVS Amino-acid Change
ENST00000299506.3:c.91-195_91-193del MANE Select ENSP00000299506.3:n.91-195_91-193del
ENST00000299506.2:c.91-195_91-193del ENSP00000299506.2:n.91-195_91-193del
ENST00000305253.8:c.256-195_256-193del ENSP00000305426.4:n.256-195_256-193del
ENST00000534099.5:c.109-195_109-193del ENSP00000434400.1:n.109-195_109-193del
NM_003320.4:c.256-195_256-193del NP_003311.2:n.256-195_256-193del
NM_177972.2:c.91-195_91-193del NP_813977.1:n.91-195_91-193del
XM_005253109.2:c.217-195_217-193del XP_005253166.1:n.217-195_217-193del
XM_011520344.1:c.127-195_127-193del XP_011518646.1:n.127-195_127-193del
XM_005253109.3:c.217-195_217-193del XP_005253166.1:n.217-195_217-193del
XM_011520344.2:c.127-195_127-193del XP_011518646.1:n.127-195_127-193del
NM_177972.3:c.91-195_91-193del MANE Select NP_813977.1:n.91-195_91-193del
NM_003320.5:c.256-195_256-193del NP_003311.2:n.256-195_256-193del