Canonical Allele Identifier: CA1950953338

Gene: TUB

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.8090102C= , CM000673.2:g.8090102C=	GRCh38
NC_000011.9:g.8111649C= , CM000673.1:g.8111649C=	GRCh37
NC_000011.8:g.8068225C=	NCBI36
NG_029912.1:g.56470C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299506.3:c.124C= MANE Select	ENSP00000299506.3:p.Arg42=
ENST00000299506.2:c.124C=	ENSP00000299506.2:p.Arg42=
ENST00000305253.8:c.289C=	ENSP00000305426.4:p.Arg97=
ENST00000534099.5:c.142C=	ENSP00000434400.1:p.Arg48=
NM_003320.4:c.289C=	NP_003311.2:p.Arg97=
NM_177972.2:c.124C=	NP_813977.1:p.Arg42=
XM_005253109.2:c.250C=	XP_005253166.1:p.Arg84=
XM_011520344.1:c.160C=	XP_011518646.1:p.Arg54=
XM_005253109.3:c.250C=	XP_005253166.1:p.Arg84=
XM_011520344.2:c.160C=	XP_011518646.1:p.Arg54=
NM_177972.3:c.124C= MANE Select	NP_813977.1:p.Arg42=
NM_003320.5:c.289C=	NP_003311.2:p.Arg97=