Canonical Allele Identifier: CA379562383
Gene: TUB HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.8089644C>T , CM000673.2:g.8089644C>T GRCh38
NC_000011.9:g.8111191C>T , CM000673.1:g.8111191C>T GRCh37
NC_000011.8:g.8067767C>T NCBI36
NG_029912.1:g.56012C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000299506.3:c.73C>T MANE Select ENSP00000299506.3:p.Gln25Ter
ENST00000299506.2:c.73C>T ENSP00000299506.2:p.Gln25Ter
ENST00000305253.8:c.238C>T ENSP00000305426.4:p.Gln80Ter
ENST00000534099.5:c.91C>T ENSP00000434400.1:p.Gln31Ter
NM_003320.4:c.238C>T NP_003311.2:p.Gln80Ter
NM_177972.2:c.73C>T NP_813977.1:p.Gln25Ter
XM_005253109.2:c.199C>T XP_005253166.1:p.Gln67Ter
XM_011520344.1:c.109C>T XP_011518646.1:p.Gln37Ter
XM_005253109.3:c.199C>T XP_005253166.1:p.Gln67Ter
XM_011520344.2:c.109C>T XP_011518646.1:p.Gln37Ter
NM_177972.3:c.73C>T MANE Select NP_813977.1:p.Gln25Ter
NM_003320.5:c.238C>T NP_003311.2:p.Gln80Ter