Canonical Allele Identifier: CA1950953156

Gene: TUB

Linked Data

• dbSNP Id: rs1943739849
• gnomAD v4: 11-8089980-G-A

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.8089980G>A , CM000673.2:g.8089980G>A	GRCh38
NC_000011.9:g.8111527G>A , CM000673.1:g.8111527G>A	GRCh37
NC_000011.8:g.8068103G>A	NCBI36
NG_029912.1:g.56348G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299506.3:c.91-89G>A MANE Select	ENSP00000299506.3:n.91-89G>A
ENST00000299506.2:c.91-89G>A	ENSP00000299506.2:n.91-89G>A
ENST00000305253.8:c.256-89G>A	ENSP00000305426.4:n.256-89G>A
ENST00000534099.5:c.109-89G>A	ENSP00000434400.1:n.109-89G>A
NM_003320.4:c.256-89G>A	NP_003311.2:n.256-89G>A
NM_177972.2:c.91-89G>A	NP_813977.1:n.91-89G>A
XM_005253109.2:c.217-89G>A	XP_005253166.1:n.217-89G>A
XM_011520344.1:c.127-89G>A	XP_011518646.1:n.127-89G>A
XM_005253109.3:c.217-89G>A	XP_005253166.1:n.217-89G>A
XM_011520344.2:c.127-89G>A	XP_011518646.1:n.127-89G>A
NM_177972.3:c.91-89G>A MANE Select	NP_813977.1:n.91-89G>A
NM_003320.5:c.256-89G>A	NP_003311.2:n.256-89G>A