Canonical Allele Identifier: CA2790351786

Gene: TUB

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.8089808_8089809insACTA , CM000673.2:g.8089808_8089809insACTA	GRCh38
NC_000011.9:g.8111355_8111356insACTA , CM000673.1:g.8111355_8111356insACTA	GRCh37
NC_000011.8:g.8067931_8067932insACTA	NCBI36
NG_029912.1:g.56176_56177insACTA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299506.3:c.90+147_90+148insACTA MANE Select	ENSP00000299506.3:n.90+147_90+148insACTA
ENST00000299506.2:c.90+147_90+148insACTA	ENSP00000299506.2:n.90+147_90+148insACTA
ENST00000305253.8:c.255+147_255+148insACTA	ENSP00000305426.4:n.255+147_255+148insACTA
ENST00000534099.5:c.108+147_108+148insACTA	ENSP00000434400.1:n.108+147_108+148insACTA
NM_003320.4:c.255+147_255+148insACTA	NP_003311.2:n.255+147_255+148insACTA
NM_177972.2:c.90+147_90+148insACTA	NP_813977.1:n.90+147_90+148insACTA
XM_005253109.2:c.216+147_216+148insACTA	XP_005253166.1:n.216+147_216+148insACTA
XM_011520344.1:c.126+147_126+148insACTA	XP_011518646.1:n.126+147_126+148insACTA
XM_005253109.3:c.216+147_216+148insACTA	XP_005253166.1:n.216+147_216+148insACTA
XM_011520344.2:c.126+147_126+148insACTA	XP_011518646.1:n.126+147_126+148insACTA
NM_177972.3:c.90+147_90+148insACTA MANE Select	NP_813977.1:n.90+147_90+148insACTA
NM_003320.5:c.255+147_255+148insACTA	NP_003311.2:n.255+147_255+148insACTA