Canonical Allele Identifier: CA473009078

Gene: TUB

Linked Data

• MyVariant Identifiers: chr11:g.8111693C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.8090146C>A , CM000673.2:g.8090146C>A	GRCh38
NC_000011.9:g.8111693C>A , CM000673.1:g.8111693C>A	GRCh37
NC_000011.8:g.8068269C>A	NCBI36
NG_029912.1:g.56514C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299506.3:c.168C>A MANE Select	ENSP00000299506.3:p.Pro56=
ENST00000299506.2:c.168C>A	ENSP00000299506.2:p.Pro56=
ENST00000305253.8:c.333C>A	ENSP00000305426.4:p.Pro111=
ENST00000534099.5:c.186C>A	ENSP00000434400.1:p.Pro62=
NM_003320.4:c.333C>A	NP_003311.2:p.Pro111=
NM_177972.2:c.168C>A	NP_813977.1:p.Pro56=
XM_005253109.2:c.294C>A	XP_005253166.1:p.Pro98=
XM_011520344.1:c.204C>A	XP_011518646.1:p.Pro68=
XM_005253109.3:c.294C>A	XP_005253166.1:p.Pro98=
XM_011520344.2:c.204C>A	XP_011518646.1:p.Pro68=
NM_177972.3:c.168C>A MANE Select	NP_813977.1:p.Pro56=
NM_003320.5:c.333C>A	NP_003311.2:p.Pro111=