Canonical Allele Identifier: CA2790351783

Gene: TUB

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.8089809_8089817del , CM000673.2:g.8089809_8089817del	GRCh38
NC_000011.9:g.8111356_8111364del , CM000673.1:g.8111356_8111364del	GRCh37
NC_000011.8:g.8067932_8067940del	NCBI36
NG_029912.1:g.56177_56185del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299506.3:c.90+148_90+156del MANE Select	ENSP00000299506.3:n.90+148_90+156del
ENST00000299506.2:c.90+148_90+156del	ENSP00000299506.2:n.90+148_90+156del
ENST00000305253.8:c.255+148_255+156del	ENSP00000305426.4:n.255+148_255+156del
ENST00000534099.5:c.108+148_108+156del	ENSP00000434400.1:n.108+148_108+156del
NM_003320.4:c.255+148_255+156del	NP_003311.2:n.255+148_255+156del
NM_177972.2:c.90+148_90+156del	NP_813977.1:n.90+148_90+156del
XM_005253109.2:c.216+148_216+156del	XP_005253166.1:n.216+148_216+156del
XM_011520344.1:c.126+148_126+156del	XP_011518646.1:n.126+148_126+156del
XM_005253109.3:c.216+148_216+156del	XP_005253166.1:n.216+148_216+156del
XM_011520344.2:c.126+148_126+156del	XP_011518646.1:n.126+148_126+156del
NM_177972.3:c.90+148_90+156del MANE Select	NP_813977.1:n.90+148_90+156del
NM_003320.5:c.255+148_255+156del	NP_003311.2:n.255+148_255+156del