Canonical Allele Identifier: CA2790351753

Gene: TUB

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.8089772_8089773insT , CM000673.2:g.8089772_8089773insT	GRCh38
NC_000011.9:g.8111319_8111320insT , CM000673.1:g.8111319_8111320insT	GRCh37
NC_000011.8:g.8067895_8067896insT	NCBI36
NG_029912.1:g.56140_56141insT

Transcript Alleles

HGVS	Amino-acid change
ENST00000299506.3:c.90+111_90+112insT MANE Select	ENSP00000299506.3:n.90+111_90+112insT
ENST00000299506.2:c.90+111_90+112insT	ENSP00000299506.2:n.90+111_90+112insT
ENST00000305253.8:c.255+111_255+112insT	ENSP00000305426.4:n.255+111_255+112insT
ENST00000534099.5:c.108+111_108+112insT	ENSP00000434400.1:n.108+111_108+112insT
NM_003320.4:c.255+111_255+112insT	NP_003311.2:n.255+111_255+112insT
NM_177972.2:c.90+111_90+112insT	NP_813977.1:n.90+111_90+112insT
XM_005253109.2:c.216+111_216+112insT	XP_005253166.1:n.216+111_216+112insT
XM_011520344.1:c.126+111_126+112insT	XP_011518646.1:n.126+111_126+112insT
XM_005253109.3:c.216+111_216+112insT	XP_005253166.1:n.216+111_216+112insT
XM_011520344.2:c.126+111_126+112insT	XP_011518646.1:n.126+111_126+112insT
NM_177972.3:c.90+111_90+112insT MANE Select	NP_813977.1:n.90+111_90+112insT
NM_003320.5:c.255+111_255+112insT	NP_003311.2:n.255+111_255+112insT