Canonical Allele Identifier: CA1950952679

Gene: TUB

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.8089593_8089595delinsCCT , CM000673.2:g.8089593_8089595delinsCCT	GRCh38
NC_000011.9:g.8111140_8111142delinsCCT , CM000673.1:g.8111140_8111142delinsCCT	GRCh37
NC_000011.8:g.8067716_8067718delinsCCT	NCBI36
NG_029912.1:g.55961_55963delinsCCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299506.3:c.39-17_39-15delinsCCT MANE Select	ENSP00000299506.3:n.39-17_39-15delinsCCT
ENST00000299506.2:c.39-17_39-15delinsCCT	ENSP00000299506.2:n.39-17_39-15delinsCCT
ENST00000305253.8:c.204-17_204-15delinsCCT	ENSP00000305426.4:n.204-17_204-15delinsCCT
ENST00000534099.5:c.57-17_57-15delinsCCT	ENSP00000434400.1:n.57-17_57-15delinsCCT
NM_003320.4:c.204-17_204-15delinsCCT	NP_003311.2:n.204-17_204-15delinsCCT
NM_177972.2:c.39-17_39-15delinsCCT	NP_813977.1:n.39-17_39-15delinsCCT
XM_005253109.2:c.165-17_165-15delinsCCT	XP_005253166.1:n.165-17_165-15delinsCCT
XM_011520344.1:c.75-17_75-15delinsCCT	XP_011518646.1:n.75-17_75-15delinsCCT
XM_005253109.3:c.165-17_165-15delinsCCT	XP_005253166.1:n.165-17_165-15delinsCCT
XM_011520344.2:c.75-17_75-15delinsCCT	XP_011518646.1:n.75-17_75-15delinsCCT
NM_177972.3:c.39-17_39-15delinsCCT MANE Select	NP_813977.1:n.39-17_39-15delinsCCT
NM_003320.5:c.204-17_204-15delinsCCT	NP_003311.2:n.204-17_204-15delinsCCT