Canonical Allele Identifier: CA363148738
Gene: TUBB HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.30723882A>T , CM000668.2:g.30723882A>T GRCh38
NC_000006.11:g.30691659A>T , CM000668.1:g.30691659A>T GRCh37
NC_000006.10:g.30799638A>T NCBI36
NG_034142.1:g.8682A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000327892.13:c.820A>T MANE Select ENSP00000339001.7:p.Thr274Ser
ENST00000680530.1:n.1682A>T
ENST00000681421.1:n.1886A>T
ENST00000681435.1:c.604A>T ENSP00000506665.1:p.Thr202Ser
ENST00000327892.12:c.820A>T ENSP00000339001.7:p.Thr274Ser
ENST00000330914.7:c.604A>T ENSP00000365578.2:p.Thr202Ser
ENST00000396384.1:c.604A>T ENSP00000379668.1:p.Thr202Ser
ENST00000396389.5:c.766A>T ENSP00000379672.1:p.Thr256Ser
NM_001293212.1:c.880A>T NP_001280141.1:p.Thr294Ser
NM_001293213.1:c.370-156A>T NP_001280142.1:n.370-156A>T
NM_001293214.1:c.688A>T NP_001280143.1:p.Thr230Ser
NM_001293215.1:c.604A>T NP_001280144.1:p.Thr202Ser
NM_001293216.1:c.604A>T NP_001280145.1:p.Thr202Ser
NM_178014.3:c.820A>T NP_821133.1:p.Thr274Ser
NR_120608.1:n.584-57A>T
NM_178014.4:c.820A>T MANE Select NP_821133.1:p.Thr274Ser
NM_001293212.2:c.880A>T NP_001280141.1:p.Thr294Ser
NM_001293213.2:c.370-156A>T NP_001280142.1:n.370-156A>T
NM_001293214.2:c.688A>T NP_001280143.1:p.Thr230Ser
NM_001293215.2:c.604A>T NP_001280144.1:p.Thr202Ser
NM_001293216.2:c.604A>T NP_001280145.1:p.Thr202Ser
NR_120608.2:n.433-57A>T