Canonical Allele Identifier: CA2612330359

Gene: TUB

Linked Data

• gnomAD v4: 11-8089605-T-A

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.8089605T>A , CM000673.2:g.8089605T>A	GRCh38
NC_000011.9:g.8111152T>A , CM000673.1:g.8111152T>A	GRCh37
NC_000011.8:g.8067728T>A	NCBI36
NG_029912.1:g.55973T>A

Transcript Alleles

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