Canonical Allele Identifier: CA2612330582
Gene: TUB HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.8090081_8090086dup , CM000673.2:g.8090081_8090086dup GRCh38
NC_000011.9:g.8111628_8111633dup , CM000673.1:g.8111628_8111633dup GRCh37
NC_000011.8:g.8068204_8068209dup NCBI36
NG_029912.1:g.56449_56454dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000299506.3:c.103_108dup MANE Select ENSP00000299506.3:p.Gln36_Lys37insGluGln
ENST00000299506.2:c.103_108dup ENSP00000299506.2:p.Gln36_Lys37insGluGln
ENST00000305253.8:c.268_273dup ENSP00000305426.4:p.Gln91_Lys92insGluGln
ENST00000534099.5:c.121_126dup ENSP00000434400.1:p.Gln42_Lys43insGluGln
NM_003320.4:c.268_273dup NP_003311.2:p.Gln91_Lys92insGluGln
NM_177972.2:c.103_108dup NP_813977.1:p.Gln36_Lys37insGluGln
XM_005253109.2:c.229_234dup XP_005253166.1:p.Gln78_Lys79insGluGln
XM_011520344.1:c.139_144dup XP_011518646.1:p.Gln48_Lys49insGluGln
XM_005253109.3:c.229_234dup XP_005253166.1:p.Gln78_Lys79insGluGln
XM_011520344.2:c.139_144dup XP_011518646.1:p.Gln48_Lys49insGluGln
NM_177972.3:c.103_108dup MANE Select NP_813977.1:p.Gln36_Lys37insGluGln
NM_003320.5:c.268_273dup NP_003311.2:p.Gln91_Lys92insGluGln