Canonical Allele Identifier: CA2612330360
Gene: TUB HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.8089622_8089624del , CM000673.2:g.8089622_8089624del GRCh38
NC_000011.9:g.8111169_8111171del , CM000673.1:g.8111169_8111171del GRCh37
NC_000011.8:g.8067745_8067747del NCBI36
NG_029912.1:g.55990_55992del

Transcript Alleles

HGVS Amino-acid Change
ENST00000299506.3:c.51_53del MANE Select ENSP00000299506.3:p.Asp17del
ENST00000299506.2:c.51_53del ENSP00000299506.2:p.Asp17del
ENST00000305253.8:c.216_218del ENSP00000305426.4:p.Asp72del
ENST00000534099.5:c.69_71del ENSP00000434400.1:p.Asp23del
NM_003320.4:c.216_218del NP_003311.2:p.Asp72del
NM_177972.2:c.51_53del NP_813977.1:p.Asp17del
XM_005253109.2:c.177_179del XP_005253166.1:p.Asp59del
XM_011520344.1:c.87_89del XP_011518646.1:p.Asp29del
XM_005253109.3:c.177_179del XP_005253166.1:p.Asp59del
XM_011520344.2:c.87_89del XP_011518646.1:p.Asp29del
NM_177972.3:c.51_53del MANE Select NP_813977.1:p.Asp17del
NM_003320.5:c.216_218del NP_003311.2:p.Asp72del