Canonical Allele Identifier: CA217415391

Gene: TUB

Linked Data

• dbSNP Id: rs1021179114
• gnomAD v4: 11-8089998-A-AC
• MyVariant Identifiers: chr11:g.8111545_8111546insC (hg19) ; chr11:g.8089998_8089999insC (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.8090004dup , CM000673.2:g.8090004dup	GRCh38
NC_000011.9:g.8111551dup , CM000673.1:g.8111551dup	GRCh37
NC_000011.8:g.8068127dup	NCBI36
NG_029912.1:g.56372dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000299506.3:c.91-65dup MANE Select	ENSP00000299506.3:n.91-65dup
ENST00000299506.2:c.91-65dup	ENSP00000299506.2:n.91-65dup
ENST00000305253.8:c.256-65dup	ENSP00000305426.4:n.256-65dup
ENST00000534099.5:c.109-65dup	ENSP00000434400.1:n.109-65dup
NM_003320.4:c.256-65dup	NP_003311.2:n.256-65dup
NM_177972.2:c.91-65dup	NP_813977.1:n.91-65dup
XM_005253109.2:c.217-65dup	XP_005253166.1:n.217-65dup
XM_011520344.1:c.127-65dup	XP_011518646.1:n.127-65dup
XM_005253109.3:c.217-65dup	XP_005253166.1:n.217-65dup
XM_011520344.2:c.127-65dup	XP_011518646.1:n.127-65dup
NM_177972.3:c.91-65dup MANE Select	NP_813977.1:n.91-65dup
NM_003320.5:c.256-65dup	NP_003311.2:n.256-65dup