Canonical Allele Identifier: CA473008999

Gene: TUB

Linked Data

• MyVariant Identifiers: chr11:g.8111157T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.8089610T>C , CM000673.2:g.8089610T>C	GRCh38
NC_000011.9:g.8111157T>C , CM000673.1:g.8111157T>C	GRCh37
NC_000011.8:g.8067733T>C	NCBI36
NG_029912.1:g.55978T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299506.3:c.39T>C MANE Select	ENSP00000299506.3:p.Ser13=
ENST00000299506.2:c.39T>C	ENSP00000299506.2:p.Ser13=
ENST00000305253.8:c.204T>C	ENSP00000305426.4:p.Arg68=
ENST00000534099.5:c.57T>C	ENSP00000434400.1:p.Ser19=
NM_003320.4:c.204T>C	NP_003311.2:p.Arg68=
NM_177972.2:c.39T>C	NP_813977.1:p.Ser13=
XM_005253109.2:c.165T>C	XP_005253166.1:p.Ser55=
XM_011520344.1:c.75T>C	XP_011518646.1:p.Ser25=
XM_005253109.3:c.165T>C	XP_005253166.1:p.Ser55=
XM_011520344.2:c.75T>C	XP_011518646.1:p.Ser25=
NM_177972.3:c.39T>C MANE Select	NP_813977.1:p.Ser13=
NM_003320.5:c.204T>C	NP_003311.2:p.Arg68=