Canonical Allele Identifier: CA379562790

Gene: TUB

Linked Data

• dbSNP Id: rs1274453151
• gnomAD v2: 11-8111677-A-G
• gnomAD v4: 11-8090130-A-G
• MyVariant Identifiers: chr11:g.8111677A>G (hg19) ; chr11:g.8090130A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.8090130A>G , CM000673.2:g.8090130A>G	GRCh38
NC_000011.9:g.8111677A>G , CM000673.1:g.8111677A>G	GRCh37
NC_000011.8:g.8068253A>G	NCBI36
NG_029912.1:g.56498A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299506.3:c.152A>G MANE Select	ENSP00000299506.3:p.Asn51Ser
ENST00000299506.2:c.152A>G	ENSP00000299506.2:p.Asn51Ser
ENST00000305253.8:c.317A>G	ENSP00000305426.4:p.Asn106Ser
ENST00000534099.5:c.170A>G	ENSP00000434400.1:p.Asn57Ser
NM_003320.4:c.317A>G	NP_003311.2:p.Asn106Ser
NM_177972.2:c.152A>G	NP_813977.1:p.Asn51Ser
XM_005253109.2:c.278A>G	XP_005253166.1:p.Asn93Ser
XM_011520344.1:c.188A>G	XP_011518646.1:p.Asn63Ser
XM_005253109.3:c.278A>G	XP_005253166.1:p.Asn93Ser
XM_011520344.2:c.188A>G	XP_011518646.1:p.Asn63Ser
NM_177972.3:c.152A>G MANE Select	NP_813977.1:p.Asn51Ser
NM_003320.5:c.317A>G	NP_003311.2:p.Asn106Ser