Canonical Allele Identifier: CA1950953441

Gene: TUB

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.8090148G= , CM000673.2:g.8090148G=	GRCh38
NC_000011.9:g.8111695G= , CM000673.1:g.8111695G=	GRCh37
NC_000011.8:g.8068271G=	NCBI36
NG_029912.1:g.56516G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299506.3:c.170G= MANE Select	ENSP00000299506.3:p.Arg57=
ENST00000299506.2:c.170G=	ENSP00000299506.2:p.Arg57=
ENST00000305253.8:c.335G=	ENSP00000305426.4:p.Arg112=
ENST00000534099.5:c.188G=	ENSP00000434400.1:p.Arg63=
NM_003320.4:c.335G=	NP_003311.2:p.Arg112=
NM_177972.2:c.170G=	NP_813977.1:p.Arg57=
XM_005253109.2:c.296G=	XP_005253166.1:p.Arg99=
XM_011520344.1:c.206G=	XP_011518646.1:p.Arg69=
XM_005253109.3:c.296G=	XP_005253166.1:p.Arg99=
XM_011520344.2:c.206G=	XP_011518646.1:p.Arg69=
NM_177972.3:c.170G= MANE Select	NP_813977.1:p.Arg57=
NM_003320.5:c.335G=	NP_003311.2:p.Arg112=