Canonical Allele Identifier: CA1950953280

Gene: TUB

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.8090072G= , CM000673.2:g.8090072G=	GRCh38
NC_000011.9:g.8111619G= , CM000673.1:g.8111619G=	GRCh37
NC_000011.8:g.8068195G=	NCBI36
NG_029912.1:g.56440G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299506.3:c.94G= MANE Select	ENSP00000299506.3:p.Ala32=
ENST00000299506.2:c.94G=	ENSP00000299506.2:p.Ala32=
ENST00000305253.8:c.259G=	ENSP00000305426.4:p.Ala87=
ENST00000534099.5:c.112G=	ENSP00000434400.1:p.Ala38=
NM_003320.4:c.259G=	NP_003311.2:p.Ala87=
NM_177972.2:c.94G=	NP_813977.1:p.Ala32=
XM_005253109.2:c.220G=	XP_005253166.1:p.Ala74=
XM_011520344.1:c.130G=	XP_011518646.1:p.Ala44=
XM_005253109.3:c.220G=	XP_005253166.1:p.Ala74=
XM_011520344.2:c.130G=	XP_011518646.1:p.Ala44=
NM_177972.3:c.94G= MANE Select	NP_813977.1:p.Ala32=
NM_003320.5:c.259G=	NP_003311.2:p.Ala87=