Canonical Allele Identifier: CA473009068

Gene: TUB

Linked Data

• MyVariant Identifiers: chr11:g.8111681A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.8090134A>G , CM000673.2:g.8090134A>G	GRCh38
NC_000011.9:g.8111681A>G , CM000673.1:g.8111681A>G	GRCh37
NC_000011.8:g.8068257A>G	NCBI36
NG_029912.1:g.56502A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299506.3:c.156A>G MANE Select	ENSP00000299506.3:p.Ala52=
ENST00000299506.2:c.156A>G	ENSP00000299506.2:p.Ala52=
ENST00000305253.8:c.321A>G	ENSP00000305426.4:p.Ala107=
ENST00000534099.5:c.174A>G	ENSP00000434400.1:p.Ala58=
NM_003320.4:c.321A>G	NP_003311.2:p.Ala107=
NM_177972.2:c.156A>G	NP_813977.1:p.Ala52=
XM_005253109.2:c.282A>G	XP_005253166.1:p.Ala94=
XM_011520344.1:c.192A>G	XP_011518646.1:p.Ala64=
XM_005253109.3:c.282A>G	XP_005253166.1:p.Ala94=
XM_011520344.2:c.192A>G	XP_011518646.1:p.Ala64=
NM_177972.3:c.156A>G MANE Select	NP_813977.1:p.Ala52=
NM_003320.5:c.321A>G	NP_003311.2:p.Ala107=