Canonical Allele Identifier: CA379562955
Gene: TUB HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.8090172A>T , CM000673.2:g.8090172A>T GRCh38
NC_000011.9:g.8111719A>T , CM000673.1:g.8111719A>T GRCh37
NC_000011.8:g.8068295A>T NCBI36
NG_029912.1:g.56540A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000299506.3:c.194A>T MANE Select ENSP00000299506.3:p.Glu65Val
ENST00000299506.2:c.194A>T ENSP00000299506.2:p.Glu65Val
ENST00000305253.8:c.359A>T ENSP00000305426.4:p.Glu120Val
ENST00000534099.5:c.212A>T ENSP00000434400.1:p.Glu71Val
NM_003320.4:c.359A>T NP_003311.2:p.Glu120Val
NM_177972.2:c.194A>T NP_813977.1:p.Glu65Val
XM_005253109.2:c.320A>T XP_005253166.1:p.Glu107Val
XM_011520344.1:c.230A>T XP_011518646.1:p.Glu77Val
XM_005253109.3:c.320A>T XP_005253166.1:p.Glu107Val
XM_011520344.2:c.230A>T XP_011518646.1:p.Glu77Val
NM_177972.3:c.194A>T MANE Select NP_813977.1:p.Glu65Val
NM_003320.5:c.359A>T NP_003311.2:p.Glu120Val