Canonical Allele Identifier: CA1618847478
Gene: TUBB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.30723290T= , CM000668.2:g.30723290T= GRCh38
NC_000006.11:g.30691067T= , CM000668.1:g.30691067T= GRCh37
NC_000006.10:g.30799046T= NCBI36
NG_034142.1:g.8090T=

Transcript Alleles

HGVS Amino-acid change
ENST00000327892.13:c.278-50T= MANE Select ENSP00000339001.7:n.278-50T=
ENST00000680530.1:n.1140-50T=
ENST00000681421.1:n.1344-50T=
ENST00000681435.1:c.62-50T= ENSP00000506665.1:n.62-50T=
ENST00000327892.12:c.278-50T= ENSP00000339001.7:n.278-50T=
ENST00000330914.7:c.62-50T= ENSP00000365578.2:n.62-50T=
ENST00000396384.1:c.62-50T= ENSP00000379668.1:n.62-50T=
ENST00000396389.5:c.224-50T= ENSP00000379672.1:n.224-50T=
NM_001293212.1:c.338-50T= NP_001280141.1:n.338-50T=
NM_001293213.1:c.278-50T= NP_001280142.1:n.278-50T=
NM_001293214.1:c.146-50T= NP_001280143.1:n.146-50T=
NM_001293215.1:c.62-50T= NP_001280144.1:n.62-50T=
NM_001293216.1:c.62-50T= NP_001280145.1:n.62-50T=
NM_178014.3:c.278-50T= NP_821133.1:n.278-50T=
NR_120608.1:n.583+262T=
NM_178014.4:c.278-50T= MANE Select NP_821133.1:n.278-50T=
NM_001293212.2:c.338-50T= NP_001280141.1:n.338-50T=
NM_001293213.2:c.278-50T= NP_001280142.1:n.278-50T=
NM_001293214.2:c.146-50T= NP_001280143.1:n.146-50T=
NM_001293215.2:c.62-50T= NP_001280144.1:n.62-50T=
NM_001293216.2:c.62-50T= NP_001280145.1:n.62-50T=
NR_120608.2:n.432+262T=