Canonical Allele Identifier: CA363148410
Gene: TUBB HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.30723811T>C , CM000668.2:g.30723811T>C GRCh38
NC_000006.11:g.30691588T>C , CM000668.1:g.30691588T>C GRCh37
NC_000006.10:g.30799567T>C NCBI36
NG_034142.1:g.8611T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000327892.13:c.749T>C MANE Select ENSP00000339001.7:p.Leu250Pro
ENST00000680530.1:n.1611T>C
ENST00000681421.1:n.1815T>C
ENST00000681435.1:c.533T>C ENSP00000506665.1:p.Leu178Pro
ENST00000327892.12:c.749T>C ENSP00000339001.7:p.Leu250Pro
ENST00000330914.7:c.533T>C ENSP00000365578.2:p.Leu178Pro
ENST00000396384.1:c.533T>C ENSP00000379668.1:p.Leu178Pro
ENST00000396389.5:c.695T>C ENSP00000379672.1:p.Leu232Pro
NM_001293212.1:c.809T>C NP_001280141.1:p.Leu270Pro
NM_001293213.1:c.370-227T>C NP_001280142.1:n.370-227T>C
NM_001293214.1:c.617T>C NP_001280143.1:p.Leu206Pro
NM_001293215.1:c.533T>C NP_001280144.1:p.Leu178Pro
NM_001293216.1:c.533T>C NP_001280145.1:p.Leu178Pro
NM_178014.3:c.749T>C NP_821133.1:p.Leu250Pro
NR_120608.1:n.584-128T>C
NM_178014.4:c.749T>C MANE Select NP_821133.1:p.Leu250Pro
NM_001293212.2:c.809T>C NP_001280141.1:p.Leu270Pro
NM_001293213.2:c.370-227T>C NP_001280142.1:n.370-227T>C
NM_001293214.2:c.617T>C NP_001280143.1:p.Leu206Pro
NM_001293215.2:c.533T>C NP_001280144.1:p.Leu178Pro
NM_001293216.2:c.533T>C NP_001280145.1:p.Leu178Pro
NR_120608.2:n.433-128T>C