Canonical Allele Identifier: CA2790351759

Gene: TUB

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.8089786_8089787insGTC , CM000673.2:g.8089786_8089787insGTC	GRCh38
NC_000011.9:g.8111333_8111334insGTC , CM000673.1:g.8111333_8111334insGTC	GRCh37
NC_000011.8:g.8067909_8067910insGTC	NCBI36
NG_029912.1:g.56154_56155insGTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299506.3:c.90+125_90+126insGTC MANE Select	ENSP00000299506.3:n.90+125_90+126insGTC
ENST00000299506.2:c.90+125_90+126insGTC	ENSP00000299506.2:n.90+125_90+126insGTC
ENST00000305253.8:c.255+125_255+126insGTC	ENSP00000305426.4:n.255+125_255+126insGTC
ENST00000534099.5:c.108+125_108+126insGTC	ENSP00000434400.1:n.108+125_108+126insGTC
NM_003320.4:c.255+125_255+126insGTC	NP_003311.2:n.255+125_255+126insGTC
NM_177972.2:c.90+125_90+126insGTC	NP_813977.1:n.90+125_90+126insGTC
XM_005253109.2:c.216+125_216+126insGTC	XP_005253166.1:n.216+125_216+126insGTC
XM_011520344.1:c.126+125_126+126insGTC	XP_011518646.1:n.126+125_126+126insGTC
XM_005253109.3:c.216+125_216+126insGTC	XP_005253166.1:n.216+125_216+126insGTC
XM_011520344.2:c.126+125_126+126insGTC	XP_011518646.1:n.126+125_126+126insGTC
NM_177972.3:c.90+125_90+126insGTC MANE Select	NP_813977.1:n.90+125_90+126insGTC
NM_003320.5:c.255+125_255+126insGTC	NP_003311.2:n.255+125_255+126insGTC