Canonical Allele Identifier: CA1950953475

Gene: TUB

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.8090156C= , CM000673.2:g.8090156C=	GRCh38
NC_000011.9:g.8111703C= , CM000673.1:g.8111703C=	GRCh37
NC_000011.8:g.8068279C=	NCBI36
NG_029912.1:g.56524C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299506.3:c.178C= MANE Select	ENSP00000299506.3:p.Arg60=
ENST00000299506.2:c.178C=	ENSP00000299506.2:p.Arg60=
ENST00000305253.8:c.343C=	ENSP00000305426.4:p.Arg115=
ENST00000534099.5:c.196C=	ENSP00000434400.1:p.Arg66=
NM_003320.4:c.343C=	NP_003311.2:p.Arg115=
NM_177972.2:c.178C=	NP_813977.1:p.Arg60=
XM_005253109.2:c.304C=	XP_005253166.1:p.Arg102=
XM_011520344.1:c.214C=	XP_011518646.1:p.Arg72=
XM_005253109.3:c.304C=	XP_005253166.1:p.Arg102=
XM_011520344.2:c.214C=	XP_011518646.1:p.Arg72=
NM_177972.3:c.178C= MANE Select	NP_813977.1:p.Arg60=
NM_003320.5:c.343C=	NP_003311.2:p.Arg115=