Canonical Allele Identifier: CA379562944
Gene: TUB HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.8090171G>T , CM000673.2:g.8090171G>T GRCh38
NC_000011.9:g.8111718G>T , CM000673.1:g.8111718G>T GRCh37
NC_000011.8:g.8068294G>T NCBI36
NG_029912.1:g.56539G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000299506.3:c.193G>T MANE Select ENSP00000299506.3:p.Glu65Ter
ENST00000299506.2:c.193G>T ENSP00000299506.2:p.Glu65Ter
ENST00000305253.8:c.358G>T ENSP00000305426.4:p.Glu120Ter
ENST00000534099.5:c.211G>T ENSP00000434400.1:p.Glu71Ter
NM_003320.4:c.358G>T NP_003311.2:p.Glu120Ter
NM_177972.2:c.193G>T NP_813977.1:p.Glu65Ter
XM_005253109.2:c.319G>T XP_005253166.1:p.Glu107Ter
XM_011520344.1:c.229G>T XP_011518646.1:p.Glu77Ter
XM_005253109.3:c.319G>T XP_005253166.1:p.Glu107Ter
XM_011520344.2:c.229G>T XP_011518646.1:p.Glu77Ter
NM_177972.3:c.193G>T MANE Select NP_813977.1:p.Glu65Ter
NM_003320.5:c.358G>T NP_003311.2:p.Glu120Ter