Canonical Allele Identifier: CA1618847647

Gene: TUBB

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.30724211G= , CM000668.2:g.30724211G=	GRCh38
NC_000006.11:g.30691988G= , CM000668.1:g.30691988G=	GRCh37
NC_000006.10:g.30799967G=	NCBI36
NG_034142.1:g.9011G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000327892.13:c.1149G= MANE Select	ENSP00000339001.7:p.Glu383=
ENST00000680530.1:n.2011G=
ENST00000681421.1:n.2215G=
ENST00000681435.1:c.933G=	ENSP00000506665.1:p.Glu311=
ENST00000327892.12:c.1149G=	ENSP00000339001.7:p.Glu383=
ENST00000330914.7:c.933G=	ENSP00000365578.2:p.Glu311=
ENST00000396384.1:c.933G=	ENSP00000379668.1:p.Glu311=
ENST00000396389.5:c.1095G=	ENSP00000379672.1:p.Glu365=
NM_001293212.1:c.1209G=	NP_001280141.1:p.Glu403=
NM_001293213.1:c.543G=	NP_001280142.1:p.Glu181=
NM_001293214.1:c.1017G=	NP_001280143.1:p.Glu339=
NM_001293215.1:c.933G=	NP_001280144.1:p.Glu311=
NM_001293216.1:c.933G=	NP_001280145.1:p.Glu311=
NM_178014.3:c.1149G=	NP_821133.1:p.Glu383=
NR_120608.1:n.856G=
NM_178014.4:c.1149G= MANE Select	NP_821133.1:p.Glu383=
NM_001293212.2:c.1209G=	NP_001280141.1:p.Glu403=
NM_001293213.2:c.543G=	NP_001280142.1:p.Glu181=
NM_001293214.2:c.1017G=	NP_001280143.1:p.Glu339=
NM_001293215.2:c.933G=	NP_001280144.1:p.Glu311=
NM_001293216.2:c.933G=	NP_001280145.1:p.Glu311=
NR_120608.2:n.705G=