Canonical Allele Identifier: CA680746743

Gene: TUB

Linked Data

• dbSNP Id: rs1453979627
• gnomAD v3: 11-8089480-T-TGCTG
• gnomAD v4: 11-8089480-T-TGCTG
• MyVariant Identifiers: chr11:g.8111027_8111028insGCTG (hg19) ; chr11:g.8089480_8089481insGCTG (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.8089481_8089482insCTGG , CM000673.2:g.8089481_8089482insCTGG	GRCh38
NC_000011.9:g.8111028_8111029insCTGG , CM000673.1:g.8111028_8111029insCTGG	GRCh37
NC_000011.8:g.8067604_8067605insCTGG	NCBI36
NG_029912.1:g.55849_55850insCTGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299506.3:c.39-129_39-128insCTGG MANE Select	ENSP00000299506.3:n.39-129_39-128insCTGG
ENST00000299506.2:c.39-129_39-128insCTGG	ENSP00000299506.2:n.39-129_39-128insCTGG
ENST00000305253.8:c.204-129_204-128insCTGG	ENSP00000305426.4:n.204-129_204-128insCTGG
ENST00000534099.5:c.57-129_57-128insCTGG	ENSP00000434400.1:n.57-129_57-128insCTGG
NM_003320.4:c.204-129_204-128insCTGG	NP_003311.2:n.204-129_204-128insCTGG
NM_177972.2:c.39-129_39-128insCTGG	NP_813977.1:n.39-129_39-128insCTGG
XM_005253109.2:c.165-129_165-128insCTGG	XP_005253166.1:n.165-129_165-128insCTGG
XM_011520344.1:c.75-129_75-128insCTGG	XP_011518646.1:n.75-129_75-128insCTGG
XM_005253109.3:c.165-129_165-128insCTGG	XP_005253166.1:n.165-129_165-128insCTGG
XM_011520344.2:c.75-129_75-128insCTGG	XP_011518646.1:n.75-129_75-128insCTGG
NM_177972.3:c.39-129_39-128insCTGG MANE Select	NP_813977.1:n.39-129_39-128insCTGG
NM_003320.5:c.204-129_204-128insCTGG	NP_003311.2:n.204-129_204-128insCTGG