Canonical Allele Identifier: CA1950953295

Gene: TUB

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.8090088A= , CM000673.2:g.8090088A=	GRCh38
NC_000011.9:g.8111635A= , CM000673.1:g.8111635A=	GRCh37
NC_000011.8:g.8068211A=	NCBI36
NG_029912.1:g.56456A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299506.3:c.110A= MANE Select	ENSP00000299506.3:p.Lys37=
ENST00000299506.2:c.110A=	ENSP00000299506.2:p.Lys37=
ENST00000305253.8:c.275A=	ENSP00000305426.4:p.Lys92=
ENST00000534099.5:c.128A=	ENSP00000434400.1:p.Lys43=
NM_003320.4:c.275A=	NP_003311.2:p.Lys92=
NM_177972.2:c.110A=	NP_813977.1:p.Lys37=
XM_005253109.2:c.236A=	XP_005253166.1:p.Lys79=
XM_011520344.1:c.146A=	XP_011518646.1:p.Lys49=
XM_005253109.3:c.236A=	XP_005253166.1:p.Lys79=
XM_011520344.2:c.146A=	XP_011518646.1:p.Lys49=
NM_177972.3:c.110A= MANE Select	NP_813977.1:p.Lys37=
NM_003320.5:c.275A=	NP_003311.2:p.Lys92=