Canonical Allele Identifier: CA379563001

Gene: TUB

Linked Data

• gnomAD v4: 11-8090181-C-A
• MyVariant Identifiers: chr11:g.8111728C>A (hg19) ; chr11:g.8090181C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.8090181C>A , CM000673.2:g.8090181C>A	GRCh38
NC_000011.9:g.8111728C>A , CM000673.1:g.8111728C>A	GRCh37
NC_000011.8:g.8068304C>A	NCBI36
NG_029912.1:g.56549C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299506.3:c.203C>A MANE Select	ENSP00000299506.3:p.Ala68Asp
ENST00000299506.2:c.203C>A	ENSP00000299506.2:p.Ala68Asp
ENST00000305253.8:c.368C>A	ENSP00000305426.4:p.Ala123Asp
ENST00000534099.5:c.221C>A	ENSP00000434400.1:p.Ala74Asp
NM_003320.4:c.368C>A	NP_003311.2:p.Ala123Asp
NM_177972.2:c.203C>A	NP_813977.1:p.Ala68Asp
XM_005253109.2:c.329C>A	XP_005253166.1:p.Ala110Asp
XM_011520344.1:c.239C>A	XP_011518646.1:p.Ala80Asp
XM_005253109.3:c.329C>A	XP_005253166.1:p.Ala110Asp
XM_011520344.2:c.239C>A	XP_011518646.1:p.Ala80Asp
NM_177972.3:c.203C>A MANE Select	NP_813977.1:p.Ala68Asp
NM_003320.5:c.368C>A	NP_003311.2:p.Ala123Asp