Canonical Allele Identifier: CA1618847575

Gene: TUBB

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.30723812C= , CM000668.2:g.30723812C=	GRCh38
NC_000006.11:g.30691589C= , CM000668.1:g.30691589C=	GRCh37
NC_000006.10:g.30799568C=	NCBI36
NG_034142.1:g.8612C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000327892.13:c.750C= MANE Select	ENSP00000339001.7:p.Leu250=
ENST00000680530.1:n.1612C=
ENST00000681421.1:n.1816C=
ENST00000681435.1:c.534C=	ENSP00000506665.1:p.Leu178=
ENST00000327892.12:c.750C=	ENSP00000339001.7:p.Leu250=
ENST00000330914.7:c.534C=	ENSP00000365578.2:p.Leu178=
ENST00000396384.1:c.534C=	ENSP00000379668.1:p.Leu178=
ENST00000396389.5:c.696C=	ENSP00000379672.1:p.Leu232=
NM_001293212.1:c.810C=	NP_001280141.1:p.Leu270=
NM_001293213.1:c.370-226C=	NP_001280142.1:n.370-226C=
NM_001293214.1:c.618C=	NP_001280143.1:p.Leu206=
NM_001293215.1:c.534C=	NP_001280144.1:p.Leu178=
NM_001293216.1:c.534C=	NP_001280145.1:p.Leu178=
NM_178014.3:c.750C=	NP_821133.1:p.Leu250=
NR_120608.1:n.584-127C=
NM_178014.4:c.750C= MANE Select	NP_821133.1:p.Leu250=
NM_001293212.2:c.810C=	NP_001280141.1:p.Leu270=
NM_001293213.2:c.370-226C=	NP_001280142.1:n.370-226C=
NM_001293214.2:c.618C=	NP_001280143.1:p.Leu206=
NM_001293215.2:c.534C=	NP_001280144.1:p.Leu178=
NM_001293216.2:c.534C=	NP_001280145.1:p.Leu178=
NR_120608.2:n.433-127C=