Canonical Allele Identifier: CA13553598
Gene: TUB HGNC NCBI

Linked Data

dbSNP Id: rs71474962
gnomAD v2: 11-8111454-C-A
gnomAD v3: 11-8089907-C-A
gnomAD v4: 11-8089907-C-A

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.8089907C>A , CM000673.2:g.8089907C>A GRCh38
NC_000011.9:g.8111454C>A , CM000673.1:g.8111454C>A GRCh37
NC_000011.8:g.8068030C>A NCBI36
NG_029912.1:g.56275C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000299506.3:c.91-162C>A MANE Select ENSP00000299506.3:n.91-162C>A
ENST00000299506.2:c.91-162C>A ENSP00000299506.2:n.91-162C>A
ENST00000305253.8:c.256-162C>A ENSP00000305426.4:n.256-162C>A
ENST00000534099.5:c.109-162C>A ENSP00000434400.1:n.109-162C>A
NM_003320.4:c.256-162C>A NP_003311.2:n.256-162C>A
NM_177972.2:c.91-162C>A NP_813977.1:n.91-162C>A
XM_005253109.2:c.217-162C>A XP_005253166.1:n.217-162C>A
XM_011520344.1:c.127-162C>A XP_011518646.1:n.127-162C>A
XM_005253109.3:c.217-162C>A XP_005253166.1:n.217-162C>A
XM_011520344.2:c.127-162C>A XP_011518646.1:n.127-162C>A
NM_177972.3:c.91-162C>A MANE Select NP_813977.1:n.91-162C>A
NM_003320.5:c.256-162C>A NP_003311.2:n.256-162C>A