Canonical Allele Identifier: CA2790351764

Gene: TUB

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.8089794_8089795insCT , CM000673.2:g.8089794_8089795insCT	GRCh38
NC_000011.9:g.8111341_8111342insCT , CM000673.1:g.8111341_8111342insCT	GRCh37
NC_000011.8:g.8067917_8067918insCT	NCBI36
NG_029912.1:g.56162_56163insCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299506.3:c.90+133_90+134insCT MANE Select	ENSP00000299506.3:n.90+133_90+134insCT
ENST00000299506.2:c.90+133_90+134insCT	ENSP00000299506.2:n.90+133_90+134insCT
ENST00000305253.8:c.255+133_255+134insCT	ENSP00000305426.4:n.255+133_255+134insCT
ENST00000534099.5:c.108+133_108+134insCT	ENSP00000434400.1:n.108+133_108+134insCT
NM_003320.4:c.255+133_255+134insCT	NP_003311.2:n.255+133_255+134insCT
NM_177972.2:c.90+133_90+134insCT	NP_813977.1:n.90+133_90+134insCT
XM_005253109.2:c.216+133_216+134insCT	XP_005253166.1:n.216+133_216+134insCT
XM_011520344.1:c.126+133_126+134insCT	XP_011518646.1:n.126+133_126+134insCT
XM_005253109.3:c.216+133_216+134insCT	XP_005253166.1:n.216+133_216+134insCT
XM_011520344.2:c.126+133_126+134insCT	XP_011518646.1:n.126+133_126+134insCT
NM_177972.3:c.90+133_90+134insCT MANE Select	NP_813977.1:n.90+133_90+134insCT
NM_003320.5:c.255+133_255+134insCT	NP_003311.2:n.255+133_255+134insCT