Canonical Allele Identifier: CA473009052

Gene: TUB

Linked Data

• MyVariant Identifiers: chr11:g.8111657G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.8090110G>A , CM000673.2:g.8090110G>A	GRCh38
NC_000011.9:g.8111657G>A , CM000673.1:g.8111657G>A	GRCh37
NC_000011.8:g.8068233G>A	NCBI36
NG_029912.1:g.56478G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299506.3:c.132G>A MANE Select	ENSP00000299506.3:p.Glu44=
ENST00000299506.2:c.132G>A	ENSP00000299506.2:p.Glu44=
ENST00000305253.8:c.297G>A	ENSP00000305426.4:p.Glu99=
ENST00000534099.5:c.150G>A	ENSP00000434400.1:p.Glu50=
NM_003320.4:c.297G>A	NP_003311.2:p.Glu99=
NM_177972.2:c.132G>A	NP_813977.1:p.Glu44=
XM_005253109.2:c.258G>A	XP_005253166.1:p.Glu86=
XM_011520344.1:c.168G>A	XP_011518646.1:p.Glu56=
XM_005253109.3:c.258G>A	XP_005253166.1:p.Glu86=
XM_011520344.2:c.168G>A	XP_011518646.1:p.Glu56=
NM_177972.3:c.132G>A MANE Select	NP_813977.1:p.Glu44=
NM_003320.5:c.297G>A	NP_003311.2:p.Glu99=