Canonical Allele Identifier: CA1950953369

Gene: TUB

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.8090127C= , CM000673.2:g.8090127C=	GRCh38
NC_000011.9:g.8111674C= , CM000673.1:g.8111674C=	GRCh37
NC_000011.8:g.8068250C=	NCBI36
NG_029912.1:g.56495C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299506.3:c.149C= MANE Select	ENSP00000299506.3:p.Ala50=
ENST00000299506.2:c.149C=	ENSP00000299506.2:p.Ala50=
ENST00000305253.8:c.314C=	ENSP00000305426.4:p.Ala105=
ENST00000534099.5:c.167C=	ENSP00000434400.1:p.Ala56=
NM_003320.4:c.314C=	NP_003311.2:p.Ala105=
NM_177972.2:c.149C=	NP_813977.1:p.Ala50=
XM_005253109.2:c.275C=	XP_005253166.1:p.Ala92=
XM_011520344.1:c.185C=	XP_011518646.1:p.Ala62=
XM_005253109.3:c.275C=	XP_005253166.1:p.Ala92=
XM_011520344.2:c.185C=	XP_011518646.1:p.Ala62=
NM_177972.3:c.149C= MANE Select	NP_813977.1:p.Ala50=
NM_003320.5:c.314C=	NP_003311.2:p.Ala105=