Canonical Allele Identifier: CA1618847634
Gene: TUBB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.30724148G= , CM000668.2:g.30724148G= GRCh38
NC_000006.11:g.30691925G= , CM000668.1:g.30691925G= GRCh37
NC_000006.10:g.30799904G= NCBI36
NG_034142.1:g.8948G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000327892.13:c.1086G= MANE Select ENSP00000339001.7:p.Lys362=
ENST00000680530.1:n.1948G=
ENST00000681421.1:n.2152G=
ENST00000681435.1:c.870G= ENSP00000506665.1:p.Lys290=
ENST00000327892.12:c.1086G= ENSP00000339001.7:p.Lys362=
ENST00000330914.7:c.870G= ENSP00000365578.2:p.Lys290=
ENST00000396384.1:c.870G= ENSP00000379668.1:p.Lys290=
ENST00000396389.5:c.1032G= ENSP00000379672.1:p.Lys344=
NM_001293212.1:c.1146G= NP_001280141.1:p.Lys382=
NM_001293213.1:c.480G= NP_001280142.1:p.Lys160=
NM_001293214.1:c.954G= NP_001280143.1:p.Lys318=
NM_001293215.1:c.870G= NP_001280144.1:p.Lys290=
NM_001293216.1:c.870G= NP_001280145.1:p.Lys290=
NM_178014.3:c.1086G= NP_821133.1:p.Lys362=
NR_120608.1:n.793G=
NM_178014.4:c.1086G= MANE Select NP_821133.1:p.Lys362=
NM_001293212.2:c.1146G= NP_001280141.1:p.Lys382=
NM_001293213.2:c.480G= NP_001280142.1:p.Lys160=
NM_001293214.2:c.954G= NP_001280143.1:p.Lys318=
NM_001293215.2:c.870G= NP_001280144.1:p.Lys290=
NM_001293216.2:c.870G= NP_001280145.1:p.Lys290=
NR_120608.2:n.642G=