Canonical Allele Identifier: CA1950953069
Gene: TUB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.8089900G= , CM000673.2:g.8089900G= GRCh38
NC_000011.9:g.8111447G= , CM000673.1:g.8111447G= GRCh37
NC_000011.8:g.8068023G= NCBI36
NG_029912.1:g.56268G=

Transcript Alleles

HGVS Amino-acid change
ENST00000299506.3:c.91-169G= MANE Select ENSP00000299506.3:n.91-169G=
ENST00000299506.2:c.91-169G= ENSP00000299506.2:n.91-169G=
ENST00000305253.8:c.256-169G= ENSP00000305426.4:n.256-169G=
ENST00000534099.5:c.109-169G= ENSP00000434400.1:n.109-169G=
NM_003320.4:c.256-169G= NP_003311.2:n.256-169G=
NM_177972.2:c.91-169G= NP_813977.1:n.91-169G=
XM_005253109.2:c.217-169G= XP_005253166.1:n.217-169G=
XM_011520344.1:c.127-169G= XP_011518646.1:n.127-169G=
XM_005253109.3:c.217-169G= XP_005253166.1:n.217-169G=
XM_011520344.2:c.127-169G= XP_011518646.1:n.127-169G=
NM_177972.3:c.91-169G= MANE Select NP_813977.1:n.91-169G=
NM_003320.5:c.256-169G= NP_003311.2:n.256-169G=