Canonical Allele Identifier: CA1950953396

Gene: TUB

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.8090135G= , CM000673.2:g.8090135G=	GRCh38
NC_000011.9:g.8111682G= , CM000673.1:g.8111682G=	GRCh37
NC_000011.8:g.8068258G=	NCBI36
NG_029912.1:g.56503G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299506.3:c.157G= MANE Select	ENSP00000299506.3:p.Asp53=
ENST00000299506.2:c.157G=	ENSP00000299506.2:p.Asp53=
ENST00000305253.8:c.322G=	ENSP00000305426.4:p.Asp108=
ENST00000534099.5:c.175G=	ENSP00000434400.1:p.Asp59=
NM_003320.4:c.322G=	NP_003311.2:p.Asp108=
NM_177972.2:c.157G=	NP_813977.1:p.Asp53=
XM_005253109.2:c.283G=	XP_005253166.1:p.Asp95=
XM_011520344.1:c.193G=	XP_011518646.1:p.Asp65=
XM_005253109.3:c.283G=	XP_005253166.1:p.Asp95=
XM_011520344.2:c.193G=	XP_011518646.1:p.Asp65=
NM_177972.3:c.157G= MANE Select	NP_813977.1:p.Asp53=
NM_003320.5:c.322G=	NP_003311.2:p.Asp108=