Canonical Allele Identifier: CA1950952881
Gene: TUB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.8089730G= , CM000673.2:g.8089730G= GRCh38
NC_000011.9:g.8111277G= , CM000673.1:g.8111277G= GRCh37
NC_000011.8:g.8067853G= NCBI36
NG_029912.1:g.56098G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000299506.3:c.90+69G= MANE Select ENSP00000299506.3:n.90+69G=
ENST00000299506.2:c.90+69G= ENSP00000299506.2:n.90+69G=
ENST00000305253.8:c.255+69G= ENSP00000305426.4:n.255+69G=
ENST00000534099.5:c.108+69G= ENSP00000434400.1:n.108+69G=
NM_003320.4:c.255+69G= NP_003311.2:n.255+69G=
NM_177972.2:c.90+69G= NP_813977.1:n.90+69G=
XM_005253109.2:c.216+69G= XP_005253166.1:n.216+69G=
XM_011520344.1:c.126+69G= XP_011518646.1:n.126+69G=
XM_005253109.3:c.216+69G= XP_005253166.1:n.216+69G=
XM_011520344.2:c.126+69G= XP_011518646.1:n.126+69G=
NM_177972.3:c.90+69G= MANE Select NP_813977.1:n.90+69G=
NM_003320.5:c.255+69G= NP_003311.2:n.255+69G=