Canonical Allele Identifier: CA1950953487

Gene: TUB

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.8090161C= , CM000673.2:g.8090161C=	GRCh38
NC_000011.9:g.8111708C= , CM000673.1:g.8111708C=	GRCh37
NC_000011.8:g.8068284C=	NCBI36
NG_029912.1:g.56529C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299506.3:c.183C= MANE Select	ENSP00000299506.3:p.Ala61=
ENST00000299506.2:c.183C=	ENSP00000299506.2:p.Ala61=
ENST00000305253.8:c.348C=	ENSP00000305426.4:p.Ala116=
ENST00000534099.5:c.201C=	ENSP00000434400.1:p.Ala67=
NM_003320.4:c.348C=	NP_003311.2:p.Ala116=
NM_177972.2:c.183C=	NP_813977.1:p.Ala61=
XM_005253109.2:c.309C=	XP_005253166.1:p.Ala103=
XM_011520344.1:c.219C=	XP_011518646.1:p.Ala73=
XM_005253109.3:c.309C=	XP_005253166.1:p.Ala103=
XM_011520344.2:c.219C=	XP_011518646.1:p.Ala73=
NM_177972.3:c.183C= MANE Select	NP_813977.1:p.Ala61=
NM_003320.5:c.348C=	NP_003311.2:p.Ala116=