Canonical Allele Identifier: CA363149511
Gene: TUBB HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.30724017G>T , CM000668.2:g.30724017G>T GRCh38
NC_000006.11:g.30691794G>T , CM000668.1:g.30691794G>T GRCh37
NC_000006.10:g.30799773G>T NCBI36
NG_034142.1:g.8817G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000327892.13:c.955G>T MANE Select ENSP00000339001.7:p.Gly319Cys
ENST00000680530.1:n.1817G>T
ENST00000681421.1:n.2021G>T
ENST00000681435.1:c.739G>T ENSP00000506665.1:p.Gly247Cys
ENST00000327892.12:c.955G>T ENSP00000339001.7:p.Gly319Cys
ENST00000330914.7:c.739G>T ENSP00000365578.2:p.Gly247Cys
ENST00000396384.1:c.739G>T ENSP00000379668.1:p.Gly247Cys
ENST00000396389.5:c.901G>T ENSP00000379672.1:p.Gly301Cys
NM_001293212.1:c.1015G>T NP_001280141.1:p.Gly339Cys
NM_001293213.1:c.370-21G>T NP_001280142.1:n.370-21G>T
NM_001293214.1:c.823G>T NP_001280143.1:p.Gly275Cys
NM_001293215.1:c.739G>T NP_001280144.1:p.Gly247Cys
NM_001293216.1:c.739G>T NP_001280145.1:p.Gly247Cys
NM_178014.3:c.955G>T NP_821133.1:p.Gly319Cys
NR_120608.1:n.662G>T
NM_178014.4:c.955G>T MANE Select NP_821133.1:p.Gly319Cys
NM_001293212.2:c.1015G>T NP_001280141.1:p.Gly339Cys
NM_001293213.2:c.370-21G>T NP_001280142.1:n.370-21G>T
NM_001293214.2:c.823G>T NP_001280143.1:p.Gly275Cys
NM_001293215.2:c.739G>T NP_001280144.1:p.Gly247Cys
NM_001293216.2:c.739G>T NP_001280145.1:p.Gly247Cys
NR_120608.2:n.511G>T