Canonical Allele Identifier: CA363151485
Gene: TUBB HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.30724261G>C , CM000668.2:g.30724261G>C GRCh38
NC_000006.11:g.30692038G>C , CM000668.1:g.30692038G>C GRCh37
NC_000006.10:g.30800017G>C NCBI36
NG_034142.1:g.9061G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000327892.13:c.1199G>C MANE Select ENSP00000339001.7:p.Gly400Ala
ENST00000680530.1:n.2061G>C
ENST00000681421.1:n.2265G>C
ENST00000681435.1:c.983G>C ENSP00000506665.1:p.Gly328Ala
ENST00000327892.12:c.1199G>C ENSP00000339001.7:p.Gly400Ala
ENST00000330914.7:c.983G>C ENSP00000365578.2:p.Gly328Ala
ENST00000396384.1:c.983G>C ENSP00000379668.1:p.Gly328Ala
ENST00000396389.5:c.1145G>C ENSP00000379672.1:p.Gly382Ala
NM_001293212.1:c.1259G>C NP_001280141.1:p.Gly420Ala
NM_001293213.1:c.593G>C NP_001280142.1:p.Gly198Ala
NM_001293214.1:c.1067G>C NP_001280143.1:p.Gly356Ala
NM_001293215.1:c.983G>C NP_001280144.1:p.Gly328Ala
NM_001293216.1:c.983G>C NP_001280145.1:p.Gly328Ala
NM_178014.3:c.1199G>C NP_821133.1:p.Gly400Ala
NR_120608.1:n.906G>C
NM_178014.4:c.1199G>C MANE Select NP_821133.1:p.Gly400Ala
NM_001293212.2:c.1259G>C NP_001280141.1:p.Gly420Ala
NM_001293213.2:c.593G>C NP_001280142.1:p.Gly198Ala
NM_001293214.2:c.1067G>C NP_001280143.1:p.Gly356Ala
NM_001293215.2:c.983G>C NP_001280144.1:p.Gly328Ala
NM_001293216.2:c.983G>C NP_001280145.1:p.Gly328Ala
NR_120608.2:n.755G>C