Canonical Allele Identifier: CA2612330349

Gene: TUB

Linked Data

• gnomAD v4: 11-8089562-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.8089562C>A , CM000673.2:g.8089562C>A	GRCh38
NC_000011.9:g.8111109C>A , CM000673.1:g.8111109C>A	GRCh37
NC_000011.8:g.8067685C>A	NCBI36
NG_029912.1:g.55930C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299506.3:c.39-48C>A MANE Select	ENSP00000299506.3:n.39-48C>A
ENST00000299506.2:c.39-48C>A	ENSP00000299506.2:n.39-48C>A
ENST00000305253.8:c.204-48C>A	ENSP00000305426.4:n.204-48C>A
ENST00000534099.5:c.57-48C>A	ENSP00000434400.1:n.57-48C>A
NM_003320.4:c.204-48C>A	NP_003311.2:n.204-48C>A
NM_177972.2:c.39-48C>A	NP_813977.1:n.39-48C>A
XM_005253109.2:c.165-48C>A	XP_005253166.1:n.165-48C>A
XM_011520344.1:c.75-48C>A	XP_011518646.1:n.75-48C>A
XM_005253109.3:c.165-48C>A	XP_005253166.1:n.165-48C>A
XM_011520344.2:c.75-48C>A	XP_011518646.1:n.75-48C>A
NM_177972.3:c.39-48C>A MANE Select	NP_813977.1:n.39-48C>A
NM_003320.5:c.204-48C>A	NP_003311.2:n.204-48C>A