Canonical Allele Identifier: CA1950952623

Gene: TUB

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.8089541G= , CM000673.2:g.8089541G=	GRCh38
NC_000011.9:g.8111088G= , CM000673.1:g.8111088G=	GRCh37
NC_000011.8:g.8067664G=	NCBI36
NG_029912.1:g.55909G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299506.3:c.39-69G= MANE Select	ENSP00000299506.3:n.39-69G=
ENST00000299506.2:c.39-69G=	ENSP00000299506.2:n.39-69G=
ENST00000305253.8:c.204-69G=	ENSP00000305426.4:n.204-69G=
ENST00000534099.5:c.57-69G=	ENSP00000434400.1:n.57-69G=
NM_003320.4:c.204-69G=	NP_003311.2:n.204-69G=
NM_177972.2:c.39-69G=	NP_813977.1:n.39-69G=
XM_005253109.2:c.165-69G=	XP_005253166.1:n.165-69G=
XM_011520344.1:c.75-69G=	XP_011518646.1:n.75-69G=
XM_005253109.3:c.165-69G=	XP_005253166.1:n.165-69G=
XM_011520344.2:c.75-69G=	XP_011518646.1:n.75-69G=
NM_177972.3:c.39-69G= MANE Select	NP_813977.1:n.39-69G=
NM_003320.5:c.204-69G=	NP_003311.2:n.204-69G=