Canonical Allele Identifier: CA2612330338
Gene: TUB HGNC NCBI

Linked Data

gnomAD v4: 11-8089538-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.8089538G>A , CM000673.2:g.8089538G>A GRCh38
NC_000011.9:g.8111085G>A , CM000673.1:g.8111085G>A GRCh37
NC_000011.8:g.8067661G>A NCBI36
NG_029912.1:g.55906G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000299506.3:c.39-72G>A MANE Select ENSP00000299506.3:n.39-72G>A
ENST00000299506.2:c.39-72G>A ENSP00000299506.2:n.39-72G>A
ENST00000305253.8:c.204-72G>A ENSP00000305426.4:n.204-72G>A
ENST00000534099.5:c.57-72G>A ENSP00000434400.1:n.57-72G>A
NM_003320.4:c.204-72G>A NP_003311.2:n.204-72G>A
NM_177972.2:c.39-72G>A NP_813977.1:n.39-72G>A
XM_005253109.2:c.165-72G>A XP_005253166.1:n.165-72G>A
XM_011520344.1:c.75-72G>A XP_011518646.1:n.75-72G>A
XM_005253109.3:c.165-72G>A XP_005253166.1:n.165-72G>A
XM_011520344.2:c.75-72G>A XP_011518646.1:n.75-72G>A
NM_177972.3:c.39-72G>A MANE Select NP_813977.1:n.39-72G>A
NM_003320.5:c.204-72G>A NP_003311.2:n.204-72G>A