Canonical Allele Identifier: CA1950953071
Gene: TUB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.8089901C= , CM000673.2:g.8089901C= GRCh38
NC_000011.9:g.8111448C= , CM000673.1:g.8111448C= GRCh37
NC_000011.8:g.8068024C= NCBI36
NG_029912.1:g.56269C=

Transcript Alleles

HGVS Amino-acid change
ENST00000299506.3:c.91-168C= MANE Select ENSP00000299506.3:n.91-168C=
ENST00000299506.2:c.91-168C= ENSP00000299506.2:n.91-168C=
ENST00000305253.8:c.256-168C= ENSP00000305426.4:n.256-168C=
ENST00000534099.5:c.109-168C= ENSP00000434400.1:n.109-168C=
NM_003320.4:c.256-168C= NP_003311.2:n.256-168C=
NM_177972.2:c.91-168C= NP_813977.1:n.91-168C=
XM_005253109.2:c.217-168C= XP_005253166.1:n.217-168C=
XM_011520344.1:c.127-168C= XP_011518646.1:n.127-168C=
XM_005253109.3:c.217-168C= XP_005253166.1:n.217-168C=
XM_011520344.2:c.127-168C= XP_011518646.1:n.127-168C=
NM_177972.3:c.91-168C= MANE Select NP_813977.1:n.91-168C=
NM_003320.5:c.256-168C= NP_003311.2:n.256-168C=