Canonical Allele Identifier: CA363149435
Gene: TUBB HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.30724008G>A , CM000668.2:g.30724008G>A GRCh38
NC_000006.11:g.30691785G>A , CM000668.1:g.30691785G>A GRCh37
NC_000006.10:g.30799764G>A NCBI36
NG_034142.1:g.8808G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000327892.13:c.946G>A MANE Select ENSP00000339001.7:p.Val316Ile
ENST00000680530.1:n.1808G>A
ENST00000681421.1:n.2012G>A
ENST00000681435.1:c.730G>A ENSP00000506665.1:p.Val244Ile
ENST00000327892.12:c.946G>A ENSP00000339001.7:p.Val316Ile
ENST00000330914.7:c.730G>A ENSP00000365578.2:p.Val244Ile
ENST00000396384.1:c.730G>A ENSP00000379668.1:p.Val244Ile
ENST00000396389.5:c.892G>A ENSP00000379672.1:p.Val298Ile
NM_001293212.1:c.1006G>A NP_001280141.1:p.Val336Ile
NM_001293213.1:c.370-30G>A NP_001280142.1:n.370-30G>A
NM_001293214.1:c.814G>A NP_001280143.1:p.Val272Ile
NM_001293215.1:c.730G>A NP_001280144.1:p.Val244Ile
NM_001293216.1:c.730G>A NP_001280145.1:p.Val244Ile
NM_178014.3:c.946G>A NP_821133.1:p.Val316Ile
NR_120608.1:n.653G>A
NM_178014.4:c.946G>A MANE Select NP_821133.1:p.Val316Ile
NM_001293212.2:c.1006G>A NP_001280141.1:p.Val336Ile
NM_001293213.2:c.370-30G>A NP_001280142.1:n.370-30G>A
NM_001293214.2:c.814G>A NP_001280143.1:p.Val272Ile
NM_001293215.2:c.730G>A NP_001280144.1:p.Val244Ile
NM_001293216.2:c.730G>A NP_001280145.1:p.Val244Ile
NR_120608.2:n.502G>A