Canonical Allele Identifier: CA2790351866

Gene: TUB

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.8089873_8089874insACG , CM000673.2:g.8089873_8089874insACG	GRCh38
NC_000011.9:g.8111420_8111421insACG , CM000673.1:g.8111420_8111421insACG	GRCh37
NC_000011.8:g.8067996_8067997insACG	NCBI36
NG_029912.1:g.56241_56242insACG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299506.3:c.91-196_91-195insACG MANE Select	ENSP00000299506.3:n.91-196_91-195insACG
ENST00000299506.2:c.91-196_91-195insACG	ENSP00000299506.2:n.91-196_91-195insACG
ENST00000305253.8:c.256-196_256-195insACG	ENSP00000305426.4:n.256-196_256-195insACG
ENST00000534099.5:c.109-196_109-195insACG	ENSP00000434400.1:n.109-196_109-195insACG
NM_003320.4:c.256-196_256-195insACG	NP_003311.2:n.256-196_256-195insACG
NM_177972.2:c.91-196_91-195insACG	NP_813977.1:n.91-196_91-195insACG
XM_005253109.2:c.217-196_217-195insACG	XP_005253166.1:n.217-196_217-195insACG
XM_011520344.1:c.127-196_127-195insACG	XP_011518646.1:n.127-196_127-195insACG
XM_005253109.3:c.217-196_217-195insACG	XP_005253166.1:n.217-196_217-195insACG
XM_011520344.2:c.127-196_127-195insACG	XP_011518646.1:n.127-196_127-195insACG
NM_177972.3:c.91-196_91-195insACG MANE Select	NP_813977.1:n.91-196_91-195insACG
NM_003320.5:c.256-196_256-195insACG	NP_003311.2:n.256-196_256-195insACG