Canonical Allele Identifier: CA1950953251

Gene: TUB

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.8090043G= , CM000673.2:g.8090043G=	GRCh38
NC_000011.9:g.8111590G= , CM000673.1:g.8111590G=	GRCh37
NC_000011.8:g.8068166G=	NCBI36
NG_029912.1:g.56411G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000299506.3:c.91-26G= MANE Select	ENSP00000299506.3:n.91-26G=
ENST00000299506.2:c.91-26G=	ENSP00000299506.2:n.91-26G=
ENST00000305253.8:c.256-26G=	ENSP00000305426.4:n.256-26G=
ENST00000534099.5:c.109-26G=	ENSP00000434400.1:n.109-26G=
NM_003320.4:c.256-26G=	NP_003311.2:n.256-26G=
NM_177972.2:c.91-26G=	NP_813977.1:n.91-26G=
XM_005253109.2:c.217-26G=	XP_005253166.1:n.217-26G=
XM_011520344.1:c.127-26G=	XP_011518646.1:n.127-26G=
XM_005253109.3:c.217-26G=	XP_005253166.1:n.217-26G=
XM_011520344.2:c.127-26G=	XP_011518646.1:n.127-26G=
NM_177972.3:c.91-26G= MANE Select	NP_813977.1:n.91-26G=
NM_003320.5:c.256-26G=	NP_003311.2:n.256-26G=