Canonical Allele Identifier: CA2770487380
Gene: TUBB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.30723803_30723804del , CM000668.2:g.30723803_30723804del GRCh38
NC_000006.11:g.30691580_30691581del , CM000668.1:g.30691580_30691581del GRCh37
NC_000006.10:g.30799559_30799560del NCBI36
NG_034142.1:g.8603_8604del

Transcript Alleles

HGVS Amino-acid Change
ENST00000327892.13:c.741_742del MANE Select ENSP00000339001.7:p.Ala248Ter
ENST00000680530.1:n.1603_1604del
ENST00000681421.1:n.1807_1808del
ENST00000681435.1:c.525_526del ENSP00000506665.1:p.Ala176Ter
ENST00000327892.12:c.741_742del ENSP00000339001.7:p.Ala248Ter
ENST00000330914.7:c.525_526del ENSP00000365578.2:p.Ala176Ter
ENST00000396384.1:c.525_526del ENSP00000379668.1:p.Ala176Ter
ENST00000396389.5:c.687_688del ENSP00000379672.1:p.Ala230Ter
NM_001293212.1:c.801_802del NP_001280141.1:p.Ala268Ter
NM_001293213.1:c.370-235_370-234del NP_001280142.1:n.370-235_370-234del
NM_001293214.1:c.609_610del NP_001280143.1:p.Ala204Ter
NM_001293215.1:c.525_526del NP_001280144.1:p.Ala176Ter
NM_001293216.1:c.525_526del NP_001280145.1:p.Ala176Ter
NM_178014.3:c.741_742del NP_821133.1:p.Ala248Ter
NR_120608.1:n.584-136_584-135del
NM_178014.4:c.741_742del MANE Select NP_821133.1:p.Ala248Ter
NM_001293212.2:c.801_802del NP_001280141.1:p.Ala268Ter
NM_001293213.2:c.370-235_370-234del NP_001280142.1:n.370-235_370-234del
NM_001293214.2:c.609_610del NP_001280143.1:p.Ala204Ter
NM_001293215.2:c.525_526del NP_001280144.1:p.Ala176Ter
NM_001293216.2:c.525_526del NP_001280145.1:p.Ala176Ter
NR_120608.2:n.433-136_433-135del