Canonical Allele Identifier: CA379562384

Gene: TUB

Linked Data

• gnomAD v4: 11-8089644-C-G
• MyVariant Identifiers: chr11:g.8111191C>G (hg19) ; chr11:g.8089644C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.8089644C>G , CM000673.2:g.8089644C>G	GRCh38
NC_000011.9:g.8111191C>G , CM000673.1:g.8111191C>G	GRCh37
NC_000011.8:g.8067767C>G	NCBI36
NG_029912.1:g.56012C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299506.3:c.73C>G MANE Select	ENSP00000299506.3:p.Gln25Glu
ENST00000299506.2:c.73C>G	ENSP00000299506.2:p.Gln25Glu
ENST00000305253.8:c.238C>G	ENSP00000305426.4:p.Gln80Glu
ENST00000534099.5:c.91C>G	ENSP00000434400.1:p.Gln31Glu
NM_003320.4:c.238C>G	NP_003311.2:p.Gln80Glu
NM_177972.2:c.73C>G	NP_813977.1:p.Gln25Glu
XM_005253109.2:c.199C>G	XP_005253166.1:p.Gln67Glu
XM_011520344.1:c.109C>G	XP_011518646.1:p.Gln37Glu
XM_005253109.3:c.199C>G	XP_005253166.1:p.Gln67Glu
XM_011520344.2:c.109C>G	XP_011518646.1:p.Gln37Glu
NM_177972.3:c.73C>G MANE Select	NP_813977.1:p.Gln25Glu
NM_003320.5:c.238C>G	NP_003311.2:p.Gln80Glu