Canonical Allele Identifier: CA473009033

Gene: TUB

Linked Data

• MyVariant Identifiers: chr11:g.8111621C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.8090074C>T , CM000673.2:g.8090074C>T	GRCh38
NC_000011.9:g.8111621C>T , CM000673.1:g.8111621C>T	GRCh37
NC_000011.8:g.8068197C>T	NCBI36
NG_029912.1:g.56442C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299506.3:c.96C>T MANE Select	ENSP00000299506.3:p.Ala32=
ENST00000299506.2:c.96C>T	ENSP00000299506.2:p.Ala32=
ENST00000305253.8:c.261C>T	ENSP00000305426.4:p.Ala87=
ENST00000534099.5:c.114C>T	ENSP00000434400.1:p.Ala38=
NM_003320.4:c.261C>T	NP_003311.2:p.Ala87=
NM_177972.2:c.96C>T	NP_813977.1:p.Ala32=
XM_005253109.2:c.222C>T	XP_005253166.1:p.Ala74=
XM_011520344.1:c.132C>T	XP_011518646.1:p.Ala44=
XM_005253109.3:c.222C>T	XP_005253166.1:p.Ala74=
XM_011520344.2:c.132C>T	XP_011518646.1:p.Ala44=
NM_177972.3:c.96C>T MANE Select	NP_813977.1:p.Ala32=
NM_003320.5:c.261C>T	NP_003311.2:p.Ala87=