Canonical Allele Identifier: CA1950953378

Gene: TUB

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.8090130A= , CM000673.2:g.8090130A=	GRCh38
NC_000011.9:g.8111677A= , CM000673.1:g.8111677A=	GRCh37
NC_000011.8:g.8068253A=	NCBI36
NG_029912.1:g.56498A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299506.3:c.152A= MANE Select	ENSP00000299506.3:p.Asn51=
ENST00000299506.2:c.152A=	ENSP00000299506.2:p.Asn51=
ENST00000305253.8:c.317A=	ENSP00000305426.4:p.Asn106=
ENST00000534099.5:c.170A=	ENSP00000434400.1:p.Asn57=
NM_003320.4:c.317A=	NP_003311.2:p.Asn106=
NM_177972.2:c.152A=	NP_813977.1:p.Asn51=
XM_005253109.2:c.278A=	XP_005253166.1:p.Asn93=
XM_011520344.1:c.188A=	XP_011518646.1:p.Asn63=
XM_005253109.3:c.278A=	XP_005253166.1:p.Asn93=
XM_011520344.2:c.188A=	XP_011518646.1:p.Asn63=
NM_177972.3:c.152A= MANE Select	NP_813977.1:p.Asn51=
NM_003320.5:c.317A=	NP_003311.2:p.Asn106=