Canonical Allele Identifier: CA2612330328

Gene: TUB

Linked Data

• gnomAD v4: 11-8089522-C-CG

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.8089525dup , CM000673.2:g.8089525dup	GRCh38
NC_000011.9:g.8111072dup , CM000673.1:g.8111072dup	GRCh37
NC_000011.8:g.8067648dup	NCBI36
NG_029912.1:g.55893dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299506.3:c.39-85dup MANE Select	ENSP00000299506.3:n.39-85dup
ENST00000299506.2:c.39-85dup	ENSP00000299506.2:n.39-85dup
ENST00000305253.8:c.204-85dup	ENSP00000305426.4:n.204-85dup
ENST00000534099.5:c.57-85dup	ENSP00000434400.1:n.57-85dup
NM_003320.4:c.204-85dup	NP_003311.2:n.204-85dup
NM_177972.2:c.39-85dup	NP_813977.1:n.39-85dup
XM_005253109.2:c.165-85dup	XP_005253166.1:n.165-85dup
XM_011520344.1:c.75-85dup	XP_011518646.1:n.75-85dup
XM_005253109.3:c.165-85dup	XP_005253166.1:n.165-85dup
XM_011520344.2:c.75-85dup	XP_011518646.1:n.75-85dup
NM_177972.3:c.39-85dup MANE Select	NP_813977.1:n.39-85dup
NM_003320.5:c.204-85dup	NP_003311.2:n.204-85dup