Canonical Allele Identifier: CA473009073

Gene: TUB

Linked Data

• MyVariant Identifiers: chr11:g.8111688C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.8090141C>A , CM000673.2:g.8090141C>A	GRCh38
NC_000011.9:g.8111688C>A , CM000673.1:g.8111688C>A	GRCh37
NC_000011.8:g.8068264C>A	NCBI36
NG_029912.1:g.56509C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299506.3:c.163C>A MANE Select	ENSP00000299506.3:p.Arg55=
ENST00000299506.2:c.163C>A	ENSP00000299506.2:p.Arg55=
ENST00000305253.8:c.328C>A	ENSP00000305426.4:p.Arg110=
ENST00000534099.5:c.181C>A	ENSP00000434400.1:p.Arg61=
NM_003320.4:c.328C>A	NP_003311.2:p.Arg110=
NM_177972.2:c.163C>A	NP_813977.1:p.Arg55=
XM_005253109.2:c.289C>A	XP_005253166.1:p.Arg97=
XM_011520344.1:c.199C>A	XP_011518646.1:p.Arg67=
XM_005253109.3:c.289C>A	XP_005253166.1:p.Arg97=
XM_011520344.2:c.199C>A	XP_011518646.1:p.Arg67=
NM_177972.3:c.163C>A MANE Select	NP_813977.1:p.Arg55=
NM_003320.5:c.328C>A	NP_003311.2:p.Arg110=