Canonical Allele Identifier: CA379562432
Gene: TUB HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.8089655T>A , CM000673.2:g.8089655T>A GRCh38
NC_000011.9:g.8111202T>A , CM000673.1:g.8111202T>A GRCh37
NC_000011.8:g.8067778T>A NCBI36
NG_029912.1:g.56023T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000299506.3:c.84T>A MANE Select ENSP00000299506.3:p.Asp28Glu
ENST00000299506.2:c.84T>A ENSP00000299506.2:p.Asp28Glu
ENST00000305253.8:c.249T>A ENSP00000305426.4:p.Asp83Glu
ENST00000534099.5:c.102T>A ENSP00000434400.1:p.Asp34Glu
NM_003320.4:c.249T>A NP_003311.2:p.Asp83Glu
NM_177972.2:c.84T>A NP_813977.1:p.Asp28Glu
XM_005253109.2:c.210T>A XP_005253166.1:p.Asp70Glu
XM_011520344.1:c.120T>A XP_011518646.1:p.Asp40Glu
XM_005253109.3:c.210T>A XP_005253166.1:p.Asp70Glu
XM_011520344.2:c.120T>A XP_011518646.1:p.Asp40Glu
NM_177972.3:c.84T>A MANE Select NP_813977.1:p.Asp28Glu
NM_003320.5:c.249T>A NP_003311.2:p.Asp83Glu