Canonical Allele Identifier: CA363148717
Gene: TUBB HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.30723877C>A , CM000668.2:g.30723877C>A GRCh38
NC_000006.11:g.30691654C>A , CM000668.1:g.30691654C>A GRCh37
NC_000006.10:g.30799633C>A NCBI36
NG_034142.1:g.8677C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000327892.13:c.815C>A MANE Select ENSP00000339001.7:p.Pro272His
ENST00000680530.1:n.1677C>A
ENST00000681421.1:n.1881C>A
ENST00000681435.1:c.599C>A ENSP00000506665.1:p.Pro200His
ENST00000327892.12:c.815C>A ENSP00000339001.7:p.Pro272His
ENST00000330914.7:c.599C>A ENSP00000365578.2:p.Pro200His
ENST00000396384.1:c.599C>A ENSP00000379668.1:p.Pro200His
ENST00000396389.5:c.761C>A ENSP00000379672.1:p.Pro254His
NM_001293212.1:c.875C>A NP_001280141.1:p.Pro292His
NM_001293213.1:c.370-161C>A NP_001280142.1:n.370-161C>A
NM_001293214.1:c.683C>A NP_001280143.1:p.Pro228His
NM_001293215.1:c.599C>A NP_001280144.1:p.Pro200His
NM_001293216.1:c.599C>A NP_001280145.1:p.Pro200His
NM_178014.3:c.815C>A NP_821133.1:p.Pro272His
NR_120608.1:n.584-62C>A
NM_178014.4:c.815C>A MANE Select NP_821133.1:p.Pro272His
NM_001293212.2:c.875C>A NP_001280141.1:p.Pro292His
NM_001293213.2:c.370-161C>A NP_001280142.1:n.370-161C>A
NM_001293214.2:c.683C>A NP_001280143.1:p.Pro228His
NM_001293215.2:c.599C>A NP_001280144.1:p.Pro200His
NM_001293216.2:c.599C>A NP_001280145.1:p.Pro200His
NR_120608.2:n.433-62C>A