Canonical Allele Identifier: CA1950953219

Gene: TUB

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.8090019_8090020delinsCG , CM000673.2:g.8090019_8090020delinsCG	GRCh38
NC_000011.9:g.8111566_8111567delinsCG , CM000673.1:g.8111566_8111567delinsCG	GRCh37
NC_000011.8:g.8068142_8068143delinsCG	NCBI36
NG_029912.1:g.56387_56388delinsCG

Transcript Alleles

HGVS	Amino-acid change
ENST00000299506.3:c.91-50_91-49delinsCG MANE Select	ENSP00000299506.3:n.91-50_91-49delinsCG
ENST00000299506.2:c.91-50_91-49delinsCG	ENSP00000299506.2:n.91-50_91-49delinsCG
ENST00000305253.8:c.256-50_256-49delinsCG	ENSP00000305426.4:n.256-50_256-49delinsCG...
ENST00000534099.5:c.109-50_109-49delinsCG	ENSP00000434400.1:n.109-50_109-49delinsCG...
NM_003320.4:c.256-50_256-49delinsCG	NP_003311.2:n.256-50_256-49delinsCG
NM_177972.2:c.91-50_91-49delinsCG	NP_813977.1:n.91-50_91-49delinsCG
XM_005253109.2:c.217-50_217-49delinsCG	XP_005253166.1:n.217-50_217-49delinsCG
XM_011520344.1:c.127-50_127-49delinsCG	XP_011518646.1:n.127-50_127-49delinsCG
XM_005253109.3:c.217-50_217-49delinsCG	XP_005253166.1:n.217-50_217-49delinsCG
XM_011520344.2:c.127-50_127-49delinsCG	XP_011518646.1:n.127-50_127-49delinsCG
NM_177972.3:c.91-50_91-49delinsCG MANE Select	NP_813977.1:n.91-50_91-49delinsCG
NM_003320.5:c.256-50_256-49delinsCG	NP_003311.2:n.256-50_256-49delinsCG