Canonical Allele Identifier: CA379562777

Gene: TUB

Linked Data

• gnomAD v4: 11-8090127-C-G
• MyVariant Identifiers: chr11:g.8111674C>G (hg19) ; chr11:g.8090127C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.8090127C>G , CM000673.2:g.8090127C>G	GRCh38
NC_000011.9:g.8111674C>G , CM000673.1:g.8111674C>G	GRCh37
NC_000011.8:g.8068250C>G	NCBI36
NG_029912.1:g.56495C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299506.3:c.149C>G MANE Select	ENSP00000299506.3:p.Ala50Gly
ENST00000299506.2:c.149C>G	ENSP00000299506.2:p.Ala50Gly
ENST00000305253.8:c.314C>G	ENSP00000305426.4:p.Ala105Gly
ENST00000534099.5:c.167C>G	ENSP00000434400.1:p.Ala56Gly
NM_003320.4:c.314C>G	NP_003311.2:p.Ala105Gly
NM_177972.2:c.149C>G	NP_813977.1:p.Ala50Gly
XM_005253109.2:c.275C>G	XP_005253166.1:p.Ala92Gly
XM_011520344.1:c.185C>G	XP_011518646.1:p.Ala62Gly
XM_005253109.3:c.275C>G	XP_005253166.1:p.Ala92Gly
XM_011520344.2:c.185C>G	XP_011518646.1:p.Ala62Gly
NM_177972.3:c.149C>G MANE Select	NP_813977.1:p.Ala50Gly
NM_003320.5:c.314C>G	NP_003311.2:p.Ala105Gly