Canonical Allele Identifier: CA363149352
Gene: TUBB HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.30723997C>G , CM000668.2:g.30723997C>G GRCh38
NC_000006.11:g.30691774C>G , CM000668.1:g.30691774C>G GRCh37
NC_000006.10:g.30799753C>G NCBI36
NG_034142.1:g.8797C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000327892.13:c.935C>G MANE Select ENSP00000339001.7:p.Thr312Ser
ENST00000680530.1:n.1797C>G
ENST00000681421.1:n.2001C>G
ENST00000681435.1:c.719C>G ENSP00000506665.1:p.Thr240Ser
ENST00000327892.12:c.935C>G ENSP00000339001.7:p.Thr312Ser
ENST00000330914.7:c.719C>G ENSP00000365578.2:p.Thr240Ser
ENST00000396384.1:c.719C>G ENSP00000379668.1:p.Thr240Ser
ENST00000396389.5:c.881C>G ENSP00000379672.1:p.Thr294Ser
NM_001293212.1:c.995C>G NP_001280141.1:p.Thr332Ser
NM_001293213.1:c.370-41C>G NP_001280142.1:n.370-41C>G
NM_001293214.1:c.803C>G NP_001280143.1:p.Thr268Ser
NM_001293215.1:c.719C>G NP_001280144.1:p.Thr240Ser
NM_001293216.1:c.719C>G NP_001280145.1:p.Thr240Ser
NM_178014.3:c.935C>G NP_821133.1:p.Thr312Ser
NR_120608.1:n.642C>G
NM_178014.4:c.935C>G MANE Select NP_821133.1:p.Thr312Ser
NM_001293212.2:c.995C>G NP_001280141.1:p.Thr332Ser
NM_001293213.2:c.370-41C>G NP_001280142.1:n.370-41C>G
NM_001293214.2:c.803C>G NP_001280143.1:p.Thr268Ser
NM_001293215.2:c.719C>G NP_001280144.1:p.Thr240Ser
NM_001293216.2:c.719C>G NP_001280145.1:p.Thr240Ser
NR_120608.2:n.491C>G