Canonical Allele Identifier: CA379562798
Gene: TUB HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.8090133C>A , CM000673.2:g.8090133C>A GRCh38
NC_000011.9:g.8111680C>A , CM000673.1:g.8111680C>A GRCh37
NC_000011.8:g.8068256C>A NCBI36
NG_029912.1:g.56501C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000299506.3:c.155C>A MANE Select ENSP00000299506.3:p.Ala52Glu
ENST00000299506.2:c.155C>A ENSP00000299506.2:p.Ala52Glu
ENST00000305253.8:c.320C>A ENSP00000305426.4:p.Ala107Glu
ENST00000534099.5:c.173C>A ENSP00000434400.1:p.Ala58Glu
NM_003320.4:c.320C>A NP_003311.2:p.Ala107Glu
NM_177972.2:c.155C>A NP_813977.1:p.Ala52Glu
XM_005253109.2:c.281C>A XP_005253166.1:p.Ala94Glu
XM_011520344.1:c.191C>A XP_011518646.1:p.Ala64Glu
XM_005253109.3:c.281C>A XP_005253166.1:p.Ala94Glu
XM_011520344.2:c.191C>A XP_011518646.1:p.Ala64Glu
NM_177972.3:c.155C>A MANE Select NP_813977.1:p.Ala52Glu
NM_003320.5:c.320C>A NP_003311.2:p.Ala107Glu