Canonical Allele Identifier: CA1950953299

Gene: TUB

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.8090089G= , CM000673.2:g.8090089G=	GRCh38
NC_000011.9:g.8111636G= , CM000673.1:g.8111636G=	GRCh37
NC_000011.8:g.8068212G=	NCBI36
NG_029912.1:g.56457G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299506.3:c.111G= MANE Select	ENSP00000299506.3:p.Lys37=
ENST00000299506.2:c.111G=	ENSP00000299506.2:p.Lys37=
ENST00000305253.8:c.276G=	ENSP00000305426.4:p.Lys92=
ENST00000534099.5:c.129G=	ENSP00000434400.1:p.Lys43=
NM_003320.4:c.276G=	NP_003311.2:p.Lys92=
NM_177972.2:c.111G=	NP_813977.1:p.Lys37=
XM_005253109.2:c.237G=	XP_005253166.1:p.Lys79=
XM_011520344.1:c.147G=	XP_011518646.1:p.Lys49=
XM_005253109.3:c.237G=	XP_005253166.1:p.Lys79=
XM_011520344.2:c.147G=	XP_011518646.1:p.Lys49=
NM_177972.3:c.111G= MANE Select	NP_813977.1:p.Lys37=
NM_003320.5:c.276G=	NP_003311.2:p.Lys92=