Canonical Allele Identifier: CA1950953098

Gene: TUB

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.8089923_8089924delinsGT , CM000673.2:g.8089923_8089924delinsGT	GRCh38
NC_000011.9:g.8111470_8111471delinsGT , CM000673.1:g.8111470_8111471delinsGT	GRCh37
NC_000011.8:g.8068046_8068047delinsGT	NCBI36
NG_029912.1:g.56291_56292delinsGT

Transcript Alleles

HGVS	Amino-acid change
ENST00000299506.3:c.91-146_91-145delinsGT MANE Select	ENSP00000299506.3:n.91-146_91-145delinsGT...
ENST00000299506.2:c.91-146_91-145delinsGT	ENSP00000299506.2:n.91-146_91-145delinsGT...
ENST00000305253.8:c.256-146_256-145delinsGT	ENSP00000305426.4:n.256-146_256-145delins...
ENST00000534099.5:c.109-146_109-145delinsGT	ENSP00000434400.1:n.109-146_109-145delins...
NM_003320.4:c.256-146_256-145delinsGT	NP_003311.2:n.256-146_256-145delinsGT
NM_177972.2:c.91-146_91-145delinsGT	NP_813977.1:n.91-146_91-145delinsGT
XM_005253109.2:c.217-146_217-145delinsGT	XP_005253166.1:n.217-146_217-145delinsGT
XM_011520344.1:c.127-146_127-145delinsGT	XP_011518646.1:n.127-146_127-145delinsGT
XM_005253109.3:c.217-146_217-145delinsGT	XP_005253166.1:n.217-146_217-145delinsGT
XM_011520344.2:c.127-146_127-145delinsGT	XP_011518646.1:n.127-146_127-145delinsGT
NM_177972.3:c.91-146_91-145delinsGT MANE Select	NP_813977.1:n.91-146_91-145delinsGT
NM_003320.5:c.256-146_256-145delinsGT	NP_003311.2:n.256-146_256-145delinsGT