Canonical Allele Identifier: CA1950953455
Gene: TUB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.8090151G= , CM000673.2:g.8090151G= GRCh38
NC_000011.9:g.8111698G= , CM000673.1:g.8111698G= GRCh37
NC_000011.8:g.8068274G= NCBI36
NG_029912.1:g.56519G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000299506.3:c.173G= MANE Select ENSP00000299506.3:p.Ser58=
ENST00000299506.2:c.173G= ENSP00000299506.2:p.Ser58=
ENST00000305253.8:c.338G= ENSP00000305426.4:p.Ser113=
ENST00000534099.5:c.191G= ENSP00000434400.1:p.Ser64=
NM_003320.4:c.338G= NP_003311.2:p.Ser113=
NM_177972.2:c.173G= NP_813977.1:p.Ser58=
XM_005253109.2:c.299G= XP_005253166.1:p.Ser100=
XM_011520344.1:c.209G= XP_011518646.1:p.Ser70=
XM_005253109.3:c.299G= XP_005253166.1:p.Ser100=
XM_011520344.2:c.209G= XP_011518646.1:p.Ser70=
NM_177972.3:c.173G= MANE Select NP_813977.1:p.Ser58=
NM_003320.5:c.338G= NP_003311.2:p.Ser113=