Canonical Allele Identifier: CA1950953261

Gene: TUB

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.8090055_8090057delinsCTG , CM000673.2:g.8090055_8090057delinsCTG	GRCh38
NC_000011.9:g.8111602_8111604delinsCTG , CM000673.1:g.8111602_8111604delinsCTG	GRCh37
NC_000011.8:g.8068178_8068180delinsCTG	NCBI36
NG_029912.1:g.56423_56425delinsCTG

Transcript Alleles

HGVS	Amino-acid change
ENST00000299506.3:c.91-14_91-12delinsCTG MANE Select	ENSP00000299506.3:n.91-14_91-12delinsCTG
ENST00000299506.2:c.91-14_91-12delinsCTG	ENSP00000299506.2:n.91-14_91-12delinsCTG
ENST00000305253.8:c.256-14_256-12delinsCTG	ENSP00000305426.4:n.256-14_256-12delinsCT...
ENST00000534099.5:c.109-14_109-12delinsCTG	ENSP00000434400.1:n.109-14_109-12delinsCT...
NM_003320.4:c.256-14_256-12delinsCTG	NP_003311.2:n.256-14_256-12delinsCTG
NM_177972.2:c.91-14_91-12delinsCTG	NP_813977.1:n.91-14_91-12delinsCTG
XM_005253109.2:c.217-14_217-12delinsCTG	XP_005253166.1:n.217-14_217-12delinsCTG
XM_011520344.1:c.127-14_127-12delinsCTG	XP_011518646.1:n.127-14_127-12delinsCTG
XM_005253109.3:c.217-14_217-12delinsCTG	XP_005253166.1:n.217-14_217-12delinsCTG
XM_011520344.2:c.127-14_127-12delinsCTG	XP_011518646.1:n.127-14_127-12delinsCTG
NM_177972.3:c.91-14_91-12delinsCTG MANE Select	NP_813977.1:n.91-14_91-12delinsCTG
NM_003320.5:c.256-14_256-12delinsCTG	NP_003311.2:n.256-14_256-12delinsCTG