Canonical Allele Identifier: CA2790351766

Gene: TUB

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.8089795_8089796insA , CM000673.2:g.8089795_8089796insA	GRCh38
NC_000011.9:g.8111342_8111343insA , CM000673.1:g.8111342_8111343insA	GRCh37
NC_000011.8:g.8067918_8067919insA	NCBI36
NG_029912.1:g.56163_56164insA

Transcript Alleles

HGVS	Amino-acid change
ENST00000299506.3:c.90+134_90+135insA MANE Select	ENSP00000299506.3:n.90+134_90+135insA
ENST00000299506.2:c.90+134_90+135insA	ENSP00000299506.2:n.90+134_90+135insA
ENST00000305253.8:c.255+134_255+135insA	ENSP00000305426.4:n.255+134_255+135insA
ENST00000534099.5:c.108+134_108+135insA	ENSP00000434400.1:n.108+134_108+135insA
NM_003320.4:c.255+134_255+135insA	NP_003311.2:n.255+134_255+135insA
NM_177972.2:c.90+134_90+135insA	NP_813977.1:n.90+134_90+135insA
XM_005253109.2:c.216+134_216+135insA	XP_005253166.1:n.216+134_216+135insA
XM_011520344.1:c.126+134_126+135insA	XP_011518646.1:n.126+134_126+135insA
XM_005253109.3:c.216+134_216+135insA	XP_005253166.1:n.216+134_216+135insA
XM_011520344.2:c.126+134_126+135insA	XP_011518646.1:n.126+134_126+135insA
NM_177972.3:c.90+134_90+135insA MANE Select	NP_813977.1:n.90+134_90+135insA
NM_003320.5:c.255+134_255+135insA	NP_003311.2:n.255+134_255+135insA