Canonical Allele Identifier: CA2612330594

Gene: TUB

Linked Data

• gnomAD v4: 11-8090254-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.8090254C>A , CM000673.2:g.8090254C>A	GRCh38
NC_000011.9:g.8111801C>A , CM000673.1:g.8111801C>A	GRCh37
NC_000011.8:g.8068377C>A	NCBI36
NG_029912.1:g.56622C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299506.3:c.253+23C>A MANE Select	ENSP00000299506.3:n.253+23C>A
ENST00000299506.2:c.253+23C>A	ENSP00000299506.2:n.253+23C>A
ENST00000305253.8:c.418+23C>A	ENSP00000305426.4:n.418+23C>A
ENST00000534099.5:c.271+23C>A	ENSP00000434400.1:n.271+23C>A
NM_003320.4:c.418+23C>A	NP_003311.2:n.418+23C>A
NM_177972.2:c.253+23C>A	NP_813977.1:n.253+23C>A
XM_005253109.2:c.379+23C>A	XP_005253166.1:n.379+23C>A
XM_011520344.1:c.289+23C>A	XP_011518646.1:n.289+23C>A
XM_005253109.3:c.379+23C>A	XP_005253166.1:n.379+23C>A
XM_011520344.2:c.289+23C>A	XP_011518646.1:n.289+23C>A
NM_177972.3:c.253+23C>A MANE Select	NP_813977.1:n.253+23C>A
NM_003320.5:c.418+23C>A	NP_003311.2:n.418+23C>A