Canonical Allele Identifier: CA2612330344

Gene: TUB

Linked Data

• gnomAD v4: 11-8089554-C-CT

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.8089555dup , CM000673.2:g.8089555dup	GRCh38
NC_000011.9:g.8111102dup , CM000673.1:g.8111102dup	GRCh37
NC_000011.8:g.8067678dup	NCBI36
NG_029912.1:g.55923dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299506.3:c.39-55dup MANE Select	ENSP00000299506.3:n.39-55dup
ENST00000299506.2:c.39-55dup	ENSP00000299506.2:n.39-55dup
ENST00000305253.8:c.204-55dup	ENSP00000305426.4:n.204-55dup
ENST00000534099.5:c.57-55dup	ENSP00000434400.1:n.57-55dup
NM_003320.4:c.204-55dup	NP_003311.2:n.204-55dup
NM_177972.2:c.39-55dup	NP_813977.1:n.39-55dup
XM_005253109.2:c.165-55dup	XP_005253166.1:n.165-55dup
XM_011520344.1:c.75-55dup	XP_011518646.1:n.75-55dup
XM_005253109.3:c.165-55dup	XP_005253166.1:n.165-55dup
XM_011520344.2:c.75-55dup	XP_011518646.1:n.75-55dup
NM_177972.3:c.39-55dup MANE Select	NP_813977.1:n.39-55dup
NM_003320.5:c.204-55dup	NP_003311.2:n.204-55dup