Canonical Allele Identifier: CA363151687
Gene: TUBB HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.30724299A>T , CM000668.2:g.30724299A>T GRCh38
NC_000006.11:g.30692076A>T , CM000668.1:g.30692076A>T GRCh37
NC_000006.10:g.30800055A>T NCBI36
NG_034142.1:g.9099A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000327892.13:c.1237A>T MANE Select ENSP00000339001.7:p.Ser413Cys
ENST00000680530.1:n.2099A>T
ENST00000681421.1:n.2303A>T
ENST00000681435.1:c.1021A>T ENSP00000506665.1:p.Ser341Cys
ENST00000327892.12:c.1237A>T ENSP00000339001.7:p.Ser413Cys
ENST00000330914.7:c.1021A>T ENSP00000365578.2:p.Ser341Cys
ENST00000396384.1:c.1021A>T ENSP00000379668.1:p.Ser341Cys
ENST00000396389.5:c.1183A>T ENSP00000379672.1:p.Ser395Cys
NM_001293212.1:c.1297A>T NP_001280141.1:p.Ser433Cys
NM_001293213.1:c.631A>T NP_001280142.1:p.Ser211Cys
NM_001293214.1:c.1105A>T NP_001280143.1:p.Ser369Cys
NM_001293215.1:c.1021A>T NP_001280144.1:p.Ser341Cys
NM_001293216.1:c.1021A>T NP_001280145.1:p.Ser341Cys
NM_178014.3:c.1237A>T NP_821133.1:p.Ser413Cys
NR_120608.1:n.944A>T
NM_178014.4:c.1237A>T MANE Select NP_821133.1:p.Ser413Cys
NM_001293212.2:c.1297A>T NP_001280141.1:p.Ser433Cys
NM_001293213.2:c.631A>T NP_001280142.1:p.Ser211Cys
NM_001293214.2:c.1105A>T NP_001280143.1:p.Ser369Cys
NM_001293215.2:c.1021A>T NP_001280144.1:p.Ser341Cys
NM_001293216.2:c.1021A>T NP_001280145.1:p.Ser341Cys
NR_120608.2:n.793A>T