Canonical Allele Identifier: CA1950953182
Gene: TUB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.8089998_8089999delinsAC , CM000673.2:g.8089998_8089999delinsAC GRCh38
NC_000011.9:g.8111545_8111546delinsAC , CM000673.1:g.8111545_8111546delinsAC GRCh37
NC_000011.8:g.8068121_8068122delinsAC NCBI36
NG_029912.1:g.56366_56367delinsAC

Transcript Alleles

HGVS Amino-acid change
ENST00000299506.3:c.91-71_91-70delinsAC MANE Select ENSP00000299506.3:n.91-71_91-70delinsAC
ENST00000299506.2:c.91-71_91-70delinsAC ENSP00000299506.2:n.91-71_91-70delinsAC
ENST00000305253.8:c.256-71_256-70delinsAC ENSP00000305426.4:n.256-71_256-70delinsAC...
ENST00000534099.5:c.109-71_109-70delinsAC ENSP00000434400.1:n.109-71_109-70delinsAC...
NM_003320.4:c.256-71_256-70delinsAC NP_003311.2:n.256-71_256-70delinsAC
NM_177972.2:c.91-71_91-70delinsAC NP_813977.1:n.91-71_91-70delinsAC
XM_005253109.2:c.217-71_217-70delinsAC XP_005253166.1:n.217-71_217-70delinsAC
XM_011520344.1:c.127-71_127-70delinsAC XP_011518646.1:n.127-71_127-70delinsAC
XM_005253109.3:c.217-71_217-70delinsAC XP_005253166.1:n.217-71_217-70delinsAC
XM_011520344.2:c.127-71_127-70delinsAC XP_011518646.1:n.127-71_127-70delinsAC
NM_177972.3:c.91-71_91-70delinsAC MANE Select NP_813977.1:n.91-71_91-70delinsAC
NM_003320.5:c.256-71_256-70delinsAC NP_003311.2:n.256-71_256-70delinsAC