Canonical Allele Identifier: CA1950952671
Gene: TUB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.8089586_8089587delinsGA , CM000673.2:g.8089586_8089587delinsGA GRCh38
NC_000011.9:g.8111133_8111134delinsGA , CM000673.1:g.8111133_8111134delinsGA GRCh37
NC_000011.8:g.8067709_8067710delinsGA NCBI36
NG_029912.1:g.55954_55955delinsGA

Transcript Alleles

HGVS Amino-acid Change
ENST00000299506.3:c.39-24_39-23delinsGA MANE Select ENSP00000299506.3:n.39-24_39-23delinsGA
ENST00000299506.2:c.39-24_39-23delinsGA ENSP00000299506.2:n.39-24_39-23delinsGA
ENST00000305253.8:c.204-24_204-23delinsGA ENSP00000305426.4:n.204-24_204-23delinsGA
ENST00000534099.5:c.57-24_57-23delinsGA ENSP00000434400.1:n.57-24_57-23delinsGA
NM_003320.4:c.204-24_204-23delinsGA NP_003311.2:n.204-24_204-23delinsGA
NM_177972.2:c.39-24_39-23delinsGA NP_813977.1:n.39-24_39-23delinsGA
XM_005253109.2:c.165-24_165-23delinsGA XP_005253166.1:n.165-24_165-23delinsGA
XM_011520344.1:c.75-24_75-23delinsGA XP_011518646.1:n.75-24_75-23delinsGA
XM_005253109.3:c.165-24_165-23delinsGA XP_005253166.1:n.165-24_165-23delinsGA
XM_011520344.2:c.75-24_75-23delinsGA XP_011518646.1:n.75-24_75-23delinsGA
NM_177972.3:c.39-24_39-23delinsGA MANE Select NP_813977.1:n.39-24_39-23delinsGA
NM_003320.5:c.204-24_204-23delinsGA NP_003311.2:n.204-24_204-23delinsGA