Canonical Allele Identifier: CA2790351843
Gene: TUB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.8089842del , CM000673.2:g.8089842del GRCh38
NC_000011.9:g.8111389del , CM000673.1:g.8111389del GRCh37
NC_000011.8:g.8067965del NCBI36
NG_029912.1:g.56210del

Transcript Alleles

HGVS Amino-acid Change
ENST00000299506.3:c.90+181del MANE Select ENSP00000299506.3:n.90+181del
ENST00000299506.2:c.90+181del ENSP00000299506.2:n.90+181del
ENST00000305253.8:c.255+181del ENSP00000305426.4:n.255+181del
ENST00000534099.5:c.108+181del ENSP00000434400.1:n.108+181del
NM_003320.4:c.255+181del NP_003311.2:n.255+181del
NM_177972.2:c.90+181del NP_813977.1:n.90+181del
XM_005253109.2:c.216+181del XP_005253166.1:n.216+181del
XM_011520344.1:c.126+181del XP_011518646.1:n.126+181del
XM_005253109.3:c.216+181del XP_005253166.1:n.216+181del
XM_011520344.2:c.126+181del XP_011518646.1:n.126+181del
NM_177972.3:c.90+181del MANE Select NP_813977.1:n.90+181del
NM_003320.5:c.255+181del NP_003311.2:n.255+181del