Canonical Allele Identifier: CA1950953375

Gene: TUB

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.8090128C= , CM000673.2:g.8090128C=	GRCh38
NC_000011.9:g.8111675C= , CM000673.1:g.8111675C=	GRCh37
NC_000011.8:g.8068251C=	NCBI36
NG_029912.1:g.56496C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299506.3:c.150C= MANE Select	ENSP00000299506.3:p.Ala50=
ENST00000299506.2:c.150C=	ENSP00000299506.2:p.Ala50=
ENST00000305253.8:c.315C=	ENSP00000305426.4:p.Ala105=
ENST00000534099.5:c.168C=	ENSP00000434400.1:p.Ala56=
NM_003320.4:c.315C=	NP_003311.2:p.Ala105=
NM_177972.2:c.150C=	NP_813977.1:p.Ala50=
XM_005253109.2:c.276C=	XP_005253166.1:p.Ala92=
XM_011520344.1:c.186C=	XP_011518646.1:p.Ala62=
XM_005253109.3:c.276C=	XP_005253166.1:p.Ala92=
XM_011520344.2:c.186C=	XP_011518646.1:p.Ala62=
NM_177972.3:c.150C= MANE Select	NP_813977.1:p.Ala50=
NM_003320.5:c.315C=	NP_003311.2:p.Ala105=