Canonical Allele Identifier: CA1950952585

Gene: TUB

Linked Data

• dbSNP Id: rs1943730517
• gnomAD v4: 11-8089499-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.8089499C>A , CM000673.2:g.8089499C>A	GRCh38
NC_000011.9:g.8111046C>A , CM000673.1:g.8111046C>A	GRCh37
NC_000011.8:g.8067622C>A	NCBI36
NG_029912.1:g.55867C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299506.3:c.39-111C>A MANE Select	ENSP00000299506.3:n.39-111C>A
ENST00000299506.2:c.39-111C>A	ENSP00000299506.2:n.39-111C>A
ENST00000305253.8:c.204-111C>A	ENSP00000305426.4:n.204-111C>A
ENST00000534099.5:c.57-111C>A	ENSP00000434400.1:n.57-111C>A
NM_003320.4:c.204-111C>A	NP_003311.2:n.204-111C>A
NM_177972.2:c.39-111C>A	NP_813977.1:n.39-111C>A
XM_005253109.2:c.165-111C>A	XP_005253166.1:n.165-111C>A
XM_011520344.1:c.75-111C>A	XP_011518646.1:n.75-111C>A
XM_005253109.3:c.165-111C>A	XP_005253166.1:n.165-111C>A
XM_011520344.2:c.75-111C>A	XP_011518646.1:n.75-111C>A
NM_177972.3:c.39-111C>A MANE Select	NP_813977.1:n.39-111C>A
NM_003320.5:c.204-111C>A	NP_003311.2:n.204-111C>A