Canonical Allele Identifier: CA2790351756

Gene: TUB

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.8089778_8089779insAGA , CM000673.2:g.8089778_8089779insAGA	GRCh38
NC_000011.9:g.8111325_8111326insAGA , CM000673.1:g.8111325_8111326insAGA	GRCh37
NC_000011.8:g.8067901_8067902insAGA	NCBI36
NG_029912.1:g.56146_56147insAGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299506.3:c.90+117_90+118insAGA MANE Select	ENSP00000299506.3:n.90+117_90+118insAGA
ENST00000299506.2:c.90+117_90+118insAGA	ENSP00000299506.2:n.90+117_90+118insAGA
ENST00000305253.8:c.255+117_255+118insAGA	ENSP00000305426.4:n.255+117_255+118insAGA
ENST00000534099.5:c.108+117_108+118insAGA	ENSP00000434400.1:n.108+117_108+118insAGA
NM_003320.4:c.255+117_255+118insAGA	NP_003311.2:n.255+117_255+118insAGA
NM_177972.2:c.90+117_90+118insAGA	NP_813977.1:n.90+117_90+118insAGA
XM_005253109.2:c.216+117_216+118insAGA	XP_005253166.1:n.216+117_216+118insAGA
XM_011520344.1:c.126+117_126+118insAGA	XP_011518646.1:n.126+117_126+118insAGA
XM_005253109.3:c.216+117_216+118insAGA	XP_005253166.1:n.216+117_216+118insAGA
XM_011520344.2:c.126+117_126+118insAGA	XP_011518646.1:n.126+117_126+118insAGA
NM_177972.3:c.90+117_90+118insAGA MANE Select	NP_813977.1:n.90+117_90+118insAGA
NM_003320.5:c.255+117_255+118insAGA	NP_003311.2:n.255+117_255+118insAGA