Canonical Allele Identifier: CA1618847576

Gene: TUBB

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.30723818G= , CM000668.2:g.30723818G=	GRCh38
NC_000006.11:g.30691595G= , CM000668.1:g.30691595G=	GRCh37
NC_000006.10:g.30799574G=	NCBI36
NG_034142.1:g.8618G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000327892.13:c.756G= MANE Select	ENSP00000339001.7:p.Lys252=
ENST00000680530.1:n.1618G=
ENST00000681421.1:n.1822G=
ENST00000681435.1:c.540G=	ENSP00000506665.1:p.Lys180=
ENST00000327892.12:c.756G=	ENSP00000339001.7:p.Lys252=
ENST00000330914.7:c.540G=	ENSP00000365578.2:p.Lys180=
ENST00000396384.1:c.540G=	ENSP00000379668.1:p.Lys180=
ENST00000396389.5:c.702G=	ENSP00000379672.1:p.Lys234=
NM_001293212.1:c.816G=	NP_001280141.1:p.Lys272=
NM_001293213.1:c.370-220G=	NP_001280142.1:n.370-220G=
NM_001293214.1:c.624G=	NP_001280143.1:p.Lys208=
NM_001293215.1:c.540G=	NP_001280144.1:p.Lys180=
NM_001293216.1:c.540G=	NP_001280145.1:p.Lys180=
NM_178014.3:c.756G=	NP_821133.1:p.Lys252=
NR_120608.1:n.584-121G=
NM_178014.4:c.756G= MANE Select	NP_821133.1:p.Lys252=
NM_001293212.2:c.816G=	NP_001280141.1:p.Lys272=
NM_001293213.2:c.370-220G=	NP_001280142.1:n.370-220G=
NM_001293214.2:c.624G=	NP_001280143.1:p.Lys208=
NM_001293215.2:c.540G=	NP_001280144.1:p.Lys180=
NM_001293216.2:c.540G=	NP_001280145.1:p.Lys180=
NR_120608.2:n.433-121G=