Canonical Allele Identifier: CA473009029

Gene: TUB

Linked Data

• gnomAD v4: 11-8090069-C-A
• MyVariant Identifiers: chr11:g.8111616C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.8090069C>A , CM000673.2:g.8090069C>A	GRCh38
NC_000011.9:g.8111616C>A , CM000673.1:g.8111616C>A	GRCh37
NC_000011.8:g.8068192C>A	NCBI36
NG_029912.1:g.56437C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299506.3:c.91C>A MANE Select	ENSP00000299506.3:p.Arg31=
ENST00000299506.2:c.91C>A	ENSP00000299506.2:p.Arg31=
ENST00000305253.8:c.256C>A	ENSP00000305426.4:p.Arg86=
ENST00000534099.5:c.109C>A	ENSP00000434400.1:p.Arg37=
NM_003320.4:c.256C>A	NP_003311.2:p.Arg86=
NM_177972.2:c.91C>A	NP_813977.1:p.Arg31=
XM_005253109.2:c.217C>A	XP_005253166.1:p.Arg73=
XM_011520344.1:c.127C>A	XP_011518646.1:p.Arg43=
XM_005253109.3:c.217C>A	XP_005253166.1:p.Arg73=
XM_011520344.2:c.127C>A	XP_011518646.1:p.Arg43=
NM_177972.3:c.91C>A MANE Select	NP_813977.1:p.Arg31=
NM_003320.5:c.256C>A	NP_003311.2:p.Arg86=