Canonical Allele Identifier: CA1618847654

Gene: TUBB

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.30724250C= , CM000668.2:g.30724250C=	GRCh38
NC_000006.11:g.30692027C= , CM000668.1:g.30692027C=	GRCh37
NC_000006.10:g.30800006C=	NCBI36
NG_034142.1:g.9050C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000327892.13:c.1188C= MANE Select	ENSP00000339001.7:p.His396=
ENST00000680530.1:n.2050C=
ENST00000681421.1:n.2254C=
ENST00000681435.1:c.972C=	ENSP00000506665.1:p.His324=
ENST00000327892.12:c.1188C=	ENSP00000339001.7:p.His396=
ENST00000330914.7:c.972C=	ENSP00000365578.2:p.His324=
ENST00000396384.1:c.972C=	ENSP00000379668.1:p.His324=
ENST00000396389.5:c.1134C=	ENSP00000379672.1:p.His378=
NM_001293212.1:c.1248C=	NP_001280141.1:p.His416=
NM_001293213.1:c.582C=	NP_001280142.1:p.His194=
NM_001293214.1:c.1056C=	NP_001280143.1:p.His352=
NM_001293215.1:c.972C=	NP_001280144.1:p.His324=
NM_001293216.1:c.972C=	NP_001280145.1:p.His324=
NM_178014.3:c.1188C=	NP_821133.1:p.His396=
NR_120608.1:n.895C=
NM_178014.4:c.1188C= MANE Select	NP_821133.1:p.His396=
NM_001293212.2:c.1248C=	NP_001280141.1:p.His416=
NM_001293213.2:c.582C=	NP_001280142.1:p.His194=
NM_001293214.2:c.1056C=	NP_001280143.1:p.His352=
NM_001293215.2:c.972C=	NP_001280144.1:p.His324=
NM_001293216.2:c.972C=	NP_001280145.1:p.His324=
NR_120608.2:n.744C=