Canonical Allele Identifier: CA1950952506

Gene: TUB

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.8089384_8089386delinsCAG , CM000673.2:g.8089384_8089386delinsCAG	GRCh38
NC_000011.9:g.8110931_8110933delinsCAG , CM000673.1:g.8110931_8110933delinsCAG	GRCh37
NC_000011.8:g.8067507_8067509delinsCAG	NCBI36
NG_029912.1:g.55752_55754delinsCAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299506.3:c.39-226_39-224delinsCAG MANE Select	ENSP00000299506.3:n.39-226_39-224delinsCAG
ENST00000299506.2:c.39-226_39-224delinsCAG	ENSP00000299506.2:n.39-226_39-224delinsCAG
ENST00000305253.8:c.204-226_204-224delinsCAG	ENSP00000305426.4:n.204-226_204-224delinsCAG
ENST00000534099.5:c.57-226_57-224delinsCAG	ENSP00000434400.1:n.57-226_57-224delinsCAG
NM_003320.4:c.204-226_204-224delinsCAG	NP_003311.2:n.204-226_204-224delinsCAG
NM_177972.2:c.39-226_39-224delinsCAG	NP_813977.1:n.39-226_39-224delinsCAG
XM_005253109.2:c.165-226_165-224delinsCAG	XP_005253166.1:n.165-226_165-224delinsCAG
XM_011520344.1:c.75-226_75-224delinsCAG	XP_011518646.1:n.75-226_75-224delinsCAG
XM_005253109.3:c.165-226_165-224delinsCAG	XP_005253166.1:n.165-226_165-224delinsCAG
XM_011520344.2:c.75-226_75-224delinsCAG	XP_011518646.1:n.75-226_75-224delinsCAG
NM_177972.3:c.39-226_39-224delinsCAG MANE Select	NP_813977.1:n.39-226_39-224delinsCAG
NM_003320.5:c.204-226_204-224delinsCAG	NP_003311.2:n.204-226_204-224delinsCAG