Canonical Allele Identifier: CA2790351877

Gene: TUB

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.8089917_8089918insA , CM000673.2:g.8089917_8089918insA	GRCh38
NC_000011.9:g.8111464_8111465insA , CM000673.1:g.8111464_8111465insA	GRCh37
NC_000011.8:g.8068040_8068041insA	NCBI36
NG_029912.1:g.56285_56286insA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299506.3:c.91-152_91-151insA MANE Select	ENSP00000299506.3:n.91-152_91-151insA
ENST00000299506.2:c.91-152_91-151insA	ENSP00000299506.2:n.91-152_91-151insA
ENST00000305253.8:c.256-152_256-151insA	ENSP00000305426.4:n.256-152_256-151insA
ENST00000534099.5:c.109-152_109-151insA	ENSP00000434400.1:n.109-152_109-151insA
NM_003320.4:c.256-152_256-151insA	NP_003311.2:n.256-152_256-151insA
NM_177972.2:c.91-152_91-151insA	NP_813977.1:n.91-152_91-151insA
XM_005253109.2:c.217-152_217-151insA	XP_005253166.1:n.217-152_217-151insA
XM_011520344.1:c.127-152_127-151insA	XP_011518646.1:n.127-152_127-151insA
XM_005253109.3:c.217-152_217-151insA	XP_005253166.1:n.217-152_217-151insA
XM_011520344.2:c.127-152_127-151insA	XP_011518646.1:n.127-152_127-151insA
NM_177972.3:c.91-152_91-151insA MANE Select	NP_813977.1:n.91-152_91-151insA
NM_003320.5:c.256-152_256-151insA	NP_003311.2:n.256-152_256-151insA