Canonical Allele Identifier: CA1618847671

Gene: TUBB

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.30724323G= , CM000668.2:g.30724323G=	GRCh38
NC_000006.11:g.30692100G= , CM000668.1:g.30692100G=	GRCh37
NC_000006.10:g.30800079G=	NCBI36
NG_034142.1:g.9123G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000327892.13:c.1261G= MANE Select	ENSP00000339001.7:p.Glu421=
ENST00000680530.1:n.2123G=
ENST00000681421.1:n.2327G=
ENST00000681435.1:c.1045G=	ENSP00000506665.1:p.Glu349=
ENST00000327892.12:c.1261G=	ENSP00000339001.7:p.Glu421=
ENST00000330914.7:c.1045G=	ENSP00000365578.2:p.Glu349=
ENST00000396384.1:c.1045G=	ENSP00000379668.1:p.Glu349=
ENST00000396389.5:c.1207G=	ENSP00000379672.1:p.Glu403=
NM_001293212.1:c.1321G=	NP_001280141.1:p.Glu441=
NM_001293213.1:c.655G=	NP_001280142.1:p.Glu219=
NM_001293214.1:c.1129G=	NP_001280143.1:p.Glu377=
NM_001293215.1:c.1045G=	NP_001280144.1:p.Glu349=
NM_001293216.1:c.1045G=	NP_001280145.1:p.Glu349=
NM_178014.3:c.1261G=	NP_821133.1:p.Glu421=
NR_120608.1:n.968G=
NM_178014.4:c.1261G= MANE Select	NP_821133.1:p.Glu421=
NM_001293212.2:c.1321G=	NP_001280141.1:p.Glu441=
NM_001293213.2:c.655G=	NP_001280142.1:p.Glu219=
NM_001293214.2:c.1129G=	NP_001280143.1:p.Glu377=
NM_001293215.2:c.1045G=	NP_001280144.1:p.Glu349=
NM_001293216.2:c.1045G=	NP_001280145.1:p.Glu349=
NR_120608.2:n.817G=