Canonical Allele Identifier: CA217415353
Gene: TUB HGNC NCBI

Linked Data

dbSNP Id: rs993599032

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.8089911C>A , CM000673.2:g.8089911C>A GRCh38
NC_000011.9:g.8111458C>A , CM000673.1:g.8111458C>A GRCh37
NC_000011.8:g.8068034C>A NCBI36
NG_029912.1:g.56279C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000299506.3:c.91-158C>A MANE Select ENSP00000299506.3:n.91-158C>A
ENST00000299506.2:c.91-158C>A ENSP00000299506.2:n.91-158C>A
ENST00000305253.8:c.256-158C>A ENSP00000305426.4:n.256-158C>A
ENST00000534099.5:c.109-158C>A ENSP00000434400.1:n.109-158C>A
NM_003320.4:c.256-158C>A NP_003311.2:n.256-158C>A
NM_177972.2:c.91-158C>A NP_813977.1:n.91-158C>A
XM_005253109.2:c.217-158C>A XP_005253166.1:n.217-158C>A
XM_011520344.1:c.127-158C>A XP_011518646.1:n.127-158C>A
XM_005253109.3:c.217-158C>A XP_005253166.1:n.217-158C>A
XM_011520344.2:c.127-158C>A XP_011518646.1:n.127-158C>A
NM_177972.3:c.91-158C>A MANE Select NP_813977.1:n.91-158C>A
NM_003320.5:c.256-158C>A NP_003311.2:n.256-158C>A