Canonical Allele Identifier: CA597322499

Gene: TUB

Linked Data

• dbSNP Id: rs1417576485
• gnomAD v2: 11-8111258-C-CT
• gnomAD v4: 11-8089711-C-CT
• MyVariant Identifiers: chr11:g.8111258_8111259insT (hg19) ; chr11:g.8089711_8089712insT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.8089712dup , CM000673.2:g.8089712dup	GRCh38
NC_000011.9:g.8111259dup , CM000673.1:g.8111259dup	GRCh37
NC_000011.8:g.8067835dup	NCBI36
NG_029912.1:g.56080dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299506.3:c.90+51dup MANE Select	ENSP00000299506.3:n.90+51dup
ENST00000299506.2:c.90+51dup	ENSP00000299506.2:n.90+51dup
ENST00000305253.8:c.255+51dup	ENSP00000305426.4:n.255+51dup
ENST00000534099.5:c.108+51dup	ENSP00000434400.1:n.108+51dup
NM_003320.4:c.255+51dup	NP_003311.2:n.255+51dup
NM_177972.2:c.90+51dup	NP_813977.1:n.90+51dup
XM_005253109.2:c.216+51dup	XP_005253166.1:n.216+51dup
XM_011520344.1:c.126+51dup	XP_011518646.1:n.126+51dup
XM_005253109.3:c.216+51dup	XP_005253166.1:n.216+51dup
XM_011520344.2:c.126+51dup	XP_011518646.1:n.126+51dup
NM_177972.3:c.90+51dup MANE Select	NP_813977.1:n.90+51dup
NM_003320.5:c.255+51dup	NP_003311.2:n.255+51dup