Canonical Allele Identifier: CA217415099

Gene: TUB

Linked Data

• dbSNP Id: rs139035034
• COSMIC: COSM1605284
• MyVariant Identifiers: chr11:g.8111203C>A (hg19) ; chr11:g.8089656C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.8089656C>A , CM000673.2:g.8089656C>A	GRCh38
NC_000011.9:g.8111203C>A , CM000673.1:g.8111203C>A	GRCh37
NC_000011.8:g.8067779C>A	NCBI36
NG_029912.1:g.56024C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299506.3:c.85C>A MANE Select	ENSP00000299506.3:p.Arg29=
ENST00000299506.2:c.85C>A	ENSP00000299506.2:p.Arg29=
ENST00000305253.8:c.250C>A	ENSP00000305426.4:p.Arg84=
ENST00000534099.5:c.103C>A	ENSP00000434400.1:p.Arg35=
NM_003320.4:c.250C>A	NP_003311.2:p.Arg84=
NM_177972.2:c.85C>A	NP_813977.1:p.Arg29=
XM_005253109.2:c.211C>A	XP_005253166.1:p.Arg71=
XM_011520344.1:c.121C>A	XP_011518646.1:p.Arg41=
XM_005253109.3:c.211C>A	XP_005253166.1:p.Arg71=
XM_011520344.2:c.121C>A	XP_011518646.1:p.Arg41=
NM_177972.3:c.85C>A MANE Select	NP_813977.1:p.Arg29=
NM_003320.5:c.250C>A	NP_003311.2:p.Arg84=