Canonical Allele Identifier: CA2790351863

Gene: TUB

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.8089867_8089868insA , CM000673.2:g.8089867_8089868insA	GRCh38
NC_000011.9:g.8111414_8111415insA , CM000673.1:g.8111414_8111415insA	GRCh37
NC_000011.8:g.8067990_8067991insA	NCBI36
NG_029912.1:g.56235_56236insA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299506.3:c.91-202_91-201insA MANE Select	ENSP00000299506.3:n.91-202_91-201insA
ENST00000299506.2:c.91-202_91-201insA	ENSP00000299506.2:n.91-202_91-201insA
ENST00000305253.8:c.256-202_256-201insA	ENSP00000305426.4:n.256-202_256-201insA
ENST00000534099.5:c.109-202_109-201insA	ENSP00000434400.1:n.109-202_109-201insA
NM_003320.4:c.256-202_256-201insA	NP_003311.2:n.256-202_256-201insA
NM_177972.2:c.91-202_91-201insA	NP_813977.1:n.91-202_91-201insA
XM_005253109.2:c.217-202_217-201insA	XP_005253166.1:n.217-202_217-201insA
XM_011520344.1:c.127-202_127-201insA	XP_011518646.1:n.127-202_127-201insA
XM_005253109.3:c.217-202_217-201insA	XP_005253166.1:n.217-202_217-201insA
XM_011520344.2:c.127-202_127-201insA	XP_011518646.1:n.127-202_127-201insA
NM_177972.3:c.91-202_91-201insA MANE Select	NP_813977.1:n.91-202_91-201insA
NM_003320.5:c.256-202_256-201insA	NP_003311.2:n.256-202_256-201insA