Canonical Allele Identifier: CA1950953436

Gene: TUB

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.8090147C= , CM000673.2:g.8090147C=	GRCh38
NC_000011.9:g.8111694C= , CM000673.1:g.8111694C=	GRCh37
NC_000011.8:g.8068270C=	NCBI36
NG_029912.1:g.56515C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299506.3:c.169C= MANE Select	ENSP00000299506.3:p.Arg57=
ENST00000299506.2:c.169C=	ENSP00000299506.2:p.Arg57=
ENST00000305253.8:c.334C=	ENSP00000305426.4:p.Arg112=
ENST00000534099.5:c.187C=	ENSP00000434400.1:p.Arg63=
NM_003320.4:c.334C=	NP_003311.2:p.Arg112=
NM_177972.2:c.169C=	NP_813977.1:p.Arg57=
XM_005253109.2:c.295C=	XP_005253166.1:p.Arg99=
XM_011520344.1:c.205C=	XP_011518646.1:p.Arg69=
XM_005253109.3:c.295C=	XP_005253166.1:p.Arg99=
XM_011520344.2:c.205C=	XP_011518646.1:p.Arg69=
NM_177972.3:c.169C= MANE Select	NP_813977.1:p.Arg57=
NM_003320.5:c.334C=	NP_003311.2:p.Arg112=