Canonical Allele Identifier: CA363149447
Gene: TUBB HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.30724009T>G , CM000668.2:g.30724009T>G GRCh38
NC_000006.11:g.30691786T>G , CM000668.1:g.30691786T>G GRCh37
NC_000006.10:g.30799765T>G NCBI36
NG_034142.1:g.8809T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000327892.13:c.947T>G MANE Select ENSP00000339001.7:p.Val316Gly
ENST00000680530.1:n.1809T>G
ENST00000681421.1:n.2013T>G
ENST00000681435.1:c.731T>G ENSP00000506665.1:p.Val244Gly
ENST00000327892.12:c.947T>G ENSP00000339001.7:p.Val316Gly
ENST00000330914.7:c.731T>G ENSP00000365578.2:p.Val244Gly
ENST00000396384.1:c.731T>G ENSP00000379668.1:p.Val244Gly
ENST00000396389.5:c.893T>G ENSP00000379672.1:p.Val298Gly
NM_001293212.1:c.1007T>G NP_001280141.1:p.Val336Gly
NM_001293213.1:c.370-29T>G NP_001280142.1:n.370-29T>G
NM_001293214.1:c.815T>G NP_001280143.1:p.Val272Gly
NM_001293215.1:c.731T>G NP_001280144.1:p.Val244Gly
NM_001293216.1:c.731T>G NP_001280145.1:p.Val244Gly
NM_178014.3:c.947T>G NP_821133.1:p.Val316Gly
NR_120608.1:n.654T>G
NM_178014.4:c.947T>G MANE Select NP_821133.1:p.Val316Gly
NM_001293212.2:c.1007T>G NP_001280141.1:p.Val336Gly
NM_001293213.2:c.370-29T>G NP_001280142.1:n.370-29T>G
NM_001293214.2:c.815T>G NP_001280143.1:p.Val272Gly
NM_001293215.2:c.731T>G NP_001280144.1:p.Val244Gly
NM_001293216.2:c.731T>G NP_001280145.1:p.Val244Gly
NR_120608.2:n.503T>G