Canonical Allele Identifier: CA1950953278

Gene: TUB

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.8090070G= , CM000673.2:g.8090070G=	GRCh38
NC_000011.9:g.8111617G= , CM000673.1:g.8111617G=	GRCh37
NC_000011.8:g.8068193G=	NCBI36
NG_029912.1:g.56438G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299506.3:c.92G= MANE Select	ENSP00000299506.3:p.Arg31=
ENST00000299506.2:c.92G=	ENSP00000299506.2:p.Arg31=
ENST00000305253.8:c.257G=	ENSP00000305426.4:p.Arg86=
ENST00000534099.5:c.110G=	ENSP00000434400.1:p.Arg37=
NM_003320.4:c.257G=	NP_003311.2:p.Arg86=
NM_177972.2:c.92G=	NP_813977.1:p.Arg31=
XM_005253109.2:c.218G=	XP_005253166.1:p.Arg73=
XM_011520344.1:c.128G=	XP_011518646.1:p.Arg43=
XM_005253109.3:c.218G=	XP_005253166.1:p.Arg73=
XM_011520344.2:c.128G=	XP_011518646.1:p.Arg43=
NM_177972.3:c.92G= MANE Select	NP_813977.1:p.Arg31=
NM_003320.5:c.257G=	NP_003311.2:p.Arg86=