Canonical Allele Identifier: CA2790351813

Gene: TUB

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.8089826_8089827insA , CM000673.2:g.8089826_8089827insA	GRCh38
NC_000011.9:g.8111373_8111374insA , CM000673.1:g.8111373_8111374insA	GRCh37
NC_000011.8:g.8067949_8067950insA	NCBI36
NG_029912.1:g.56194_56195insA

Transcript Alleles

HGVS	Amino-acid change
ENST00000299506.3:c.90+165_90+166insA MANE Select	ENSP00000299506.3:n.90+165_90+166insA
ENST00000299506.2:c.90+165_90+166insA	ENSP00000299506.2:n.90+165_90+166insA
ENST00000305253.8:c.255+165_255+166insA	ENSP00000305426.4:n.255+165_255+166insA
ENST00000534099.5:c.108+165_108+166insA	ENSP00000434400.1:n.108+165_108+166insA
NM_003320.4:c.255+165_255+166insA	NP_003311.2:n.255+165_255+166insA
NM_177972.2:c.90+165_90+166insA	NP_813977.1:n.90+165_90+166insA
XM_005253109.2:c.216+165_216+166insA	XP_005253166.1:n.216+165_216+166insA
XM_011520344.1:c.126+165_126+166insA	XP_011518646.1:n.126+165_126+166insA
XM_005253109.3:c.216+165_216+166insA	XP_005253166.1:n.216+165_216+166insA
XM_011520344.2:c.126+165_126+166insA	XP_011518646.1:n.126+165_126+166insA
NM_177972.3:c.90+165_90+166insA MANE Select	NP_813977.1:n.90+165_90+166insA
NM_003320.5:c.255+165_255+166insA	NP_003311.2:n.255+165_255+166insA