Canonical Allele Identifier: CA379562289
Gene: TUB HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.8089623G>T , CM000673.2:g.8089623G>T GRCh38
NC_000011.9:g.8111170G>T , CM000673.1:g.8111170G>T GRCh37
NC_000011.8:g.8067746G>T NCBI36
NG_029912.1:g.55991G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000299506.3:c.52G>T MANE Select ENSP00000299506.3:p.Glu18Ter
ENST00000299506.2:c.52G>T ENSP00000299506.2:p.Glu18Ter
ENST00000305253.8:c.217G>T ENSP00000305426.4:p.Glu73Ter
ENST00000534099.5:c.70G>T ENSP00000434400.1:p.Glu24Ter
NM_003320.4:c.217G>T NP_003311.2:p.Glu73Ter
NM_177972.2:c.52G>T NP_813977.1:p.Glu18Ter
XM_005253109.2:c.178G>T XP_005253166.1:p.Glu60Ter
XM_011520344.1:c.88G>T XP_011518646.1:p.Glu30Ter
XM_005253109.3:c.178G>T XP_005253166.1:p.Glu60Ter
XM_011520344.2:c.88G>T XP_011518646.1:p.Glu30Ter
NM_177972.3:c.52G>T MANE Select NP_813977.1:p.Glu18Ter
NM_003320.5:c.217G>T NP_003311.2:p.Glu73Ter