Canonical Allele Identifier: CA1950953095
Gene: TUB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.8089920_8089922delinsCCT , CM000673.2:g.8089920_8089922delinsCCT GRCh38
NC_000011.9:g.8111467_8111469delinsCCT , CM000673.1:g.8111467_8111469delinsCCT GRCh37
NC_000011.8:g.8068043_8068045delinsCCT NCBI36
NG_029912.1:g.56288_56290delinsCCT

Transcript Alleles

HGVS Amino-acid change
ENST00000299506.3:c.91-149_91-147delinsCCT MANE Select ENSP00000299506.3:n.91-149_91-147delinsCC...
ENST00000299506.2:c.91-149_91-147delinsCCT ENSP00000299506.2:n.91-149_91-147delinsCC...
ENST00000305253.8:c.256-149_256-147delinsCCT ENSP00000305426.4:n.256-149_256-147delins...
ENST00000534099.5:c.109-149_109-147delinsCCT ENSP00000434400.1:n.109-149_109-147delins...
NM_003320.4:c.256-149_256-147delinsCCT NP_003311.2:n.256-149_256-147delinsCCT
NM_177972.2:c.91-149_91-147delinsCCT NP_813977.1:n.91-149_91-147delinsCCT
XM_005253109.2:c.217-149_217-147delinsCCT XP_005253166.1:n.217-149_217-147delinsCCT...
XM_011520344.1:c.127-149_127-147delinsCCT XP_011518646.1:n.127-149_127-147delinsCCT...
XM_005253109.3:c.217-149_217-147delinsCCT XP_005253166.1:n.217-149_217-147delinsCCT...
XM_011520344.2:c.127-149_127-147delinsCCT XP_011518646.1:n.127-149_127-147delinsCCT...
NM_177972.3:c.91-149_91-147delinsCCT MANE Select NP_813977.1:n.91-149_91-147delinsCCT
NM_003320.5:c.256-149_256-147delinsCCT NP_003311.2:n.256-149_256-147delinsCCT