Canonical Allele Identifier: CA597322372
Gene: TUB HGNC NCBI

Linked Data

dbSNP Id: rs1253241068

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.8089590del , CM000673.2:g.8089590del GRCh38
NC_000011.9:g.8111137del , CM000673.1:g.8111137del GRCh37
NC_000011.8:g.8067713del NCBI36
NG_029912.1:g.55958del

Transcript Alleles

HGVS Amino-acid Change
ENST00000299506.3:c.39-20del MANE Select ENSP00000299506.3:n.39-20del
ENST00000299506.2:c.39-20del ENSP00000299506.2:n.39-20del
ENST00000305253.8:c.204-20del ENSP00000305426.4:n.204-20del
ENST00000534099.5:c.57-20del ENSP00000434400.1:n.57-20del
NM_003320.4:c.204-20del NP_003311.2:n.204-20del
NM_177972.2:c.39-20del NP_813977.1:n.39-20del
XM_005253109.2:c.165-20del XP_005253166.1:n.165-20del
XM_011520344.1:c.75-20del XP_011518646.1:n.75-20del
XM_005253109.3:c.165-20del XP_005253166.1:n.165-20del
XM_011520344.2:c.75-20del XP_011518646.1:n.75-20del
NM_177972.3:c.39-20del MANE Select NP_813977.1:n.39-20del
NM_003320.5:c.204-20del NP_003311.2:n.204-20del