Canonical Allele Identifier: CA1950953406

Gene: TUB

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.8090139G= , CM000673.2:g.8090139G=	GRCh38
NC_000011.9:g.8111686G= , CM000673.1:g.8111686G=	GRCh37
NC_000011.8:g.8068262G=	NCBI36
NG_029912.1:g.56507G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299506.3:c.161G= MANE Select	ENSP00000299506.3:p.Gly54=
ENST00000299506.2:c.161G=	ENSP00000299506.2:p.Gly54=
ENST00000305253.8:c.326G=	ENSP00000305426.4:p.Gly109=
ENST00000534099.5:c.179G=	ENSP00000434400.1:p.Gly60=
NM_003320.4:c.326G=	NP_003311.2:p.Gly109=
NM_177972.2:c.161G=	NP_813977.1:p.Gly54=
XM_005253109.2:c.287G=	XP_005253166.1:p.Gly96=
XM_011520344.1:c.197G=	XP_011518646.1:p.Gly66=
XM_005253109.3:c.287G=	XP_005253166.1:p.Gly96=
XM_011520344.2:c.197G=	XP_011518646.1:p.Gly66=
NM_177972.3:c.161G= MANE Select	NP_813977.1:p.Gly54=
NM_003320.5:c.326G=	NP_003311.2:p.Gly109=