Canonical Allele Identifier: CA2790351890
Gene: TUB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.8090120_8090122del , CM000673.2:g.8090120_8090122del GRCh38
NC_000011.9:g.8111667_8111669del , CM000673.1:g.8111667_8111669del GRCh37
NC_000011.8:g.8068243_8068245del NCBI36
NG_029912.1:g.56488_56490del

Transcript Alleles

HGVS Amino-acid Change
ENST00000299506.3:c.142_144del MANE Select ENSP00000299506.3:p.Val48del
ENST00000299506.2:c.142_144del ENSP00000299506.2:p.Val48del
ENST00000305253.8:c.307_309del ENSP00000305426.4:p.Val103del
ENST00000534099.5:c.160_162del ENSP00000434400.1:p.Val54del
NM_003320.4:c.307_309del NP_003311.2:p.Val103del
NM_177972.2:c.142_144del NP_813977.1:p.Val48del
XM_005253109.2:c.268_270del XP_005253166.1:p.Val90del
XM_011520344.1:c.178_180del XP_011518646.1:p.Val60del
XM_005253109.3:c.268_270del XP_005253166.1:p.Val90del
XM_011520344.2:c.178_180del XP_011518646.1:p.Val60del
NM_177972.3:c.142_144del MANE Select NP_813977.1:p.Val48del
NM_003320.5:c.307_309del NP_003311.2:p.Val103del