Canonical Allele Identifier: CA379562789

Gene: TUB

Linked Data

• gnomAD v4: 11-8090130-A-T
• MyVariant Identifiers: chr11:g.8111677A>T (hg19) ; chr11:g.8090130A>T (hg38)

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299506.3:c.152A>T MANE Select	ENSP00000299506.3:p.Asn51Ile
ENST00000299506.2:c.152A>T	ENSP00000299506.2:p.Asn51Ile
ENST00000305253.8:c.317A>T	ENSP00000305426.4:p.Asn106Ile
ENST00000534099.5:c.170A>T	ENSP00000434400.1:p.Asn57Ile
NM_003320.4:c.317A>T	NP_003311.2:p.Asn106Ile
NM_177972.2:c.152A>T	NP_813977.1:p.Asn51Ile
XM_005253109.2:c.278A>T	XP_005253166.1:p.Asn93Ile
XM_011520344.1:c.188A>T	XP_011518646.1:p.Asn63Ile
XM_005253109.3:c.278A>T	XP_005253166.1:p.Asn93Ile
XM_011520344.2:c.188A>T	XP_011518646.1:p.Asn63Ile
NM_177972.3:c.152A>T MANE Select	NP_813977.1:p.Asn51Ile
NM_003320.5:c.317A>T	NP_003311.2:p.Asn106Ile