Canonical Allele Identifier: CA473009082

Gene: TUB

Linked Data

• MyVariant Identifiers: chr11:g.8111696G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.8090149G>T , CM000673.2:g.8090149G>T	GRCh38
NC_000011.9:g.8111696G>T , CM000673.1:g.8111696G>T	GRCh37
NC_000011.8:g.8068272G>T	NCBI36
NG_029912.1:g.56517G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299506.3:c.171G>T MANE Select	ENSP00000299506.3:p.Arg57=
ENST00000299506.2:c.171G>T	ENSP00000299506.2:p.Arg57=
ENST00000305253.8:c.336G>T	ENSP00000305426.4:p.Arg112=
ENST00000534099.5:c.189G>T	ENSP00000434400.1:p.Arg63=
NM_003320.4:c.336G>T	NP_003311.2:p.Arg112=
NM_177972.2:c.171G>T	NP_813977.1:p.Arg57=
XM_005253109.2:c.297G>T	XP_005253166.1:p.Arg99=
XM_011520344.1:c.207G>T	XP_011518646.1:p.Arg69=
XM_005253109.3:c.297G>T	XP_005253166.1:p.Arg99=
XM_011520344.2:c.207G>T	XP_011518646.1:p.Arg69=
NM_177972.3:c.171G>T MANE Select	NP_813977.1:p.Arg57=
NM_003320.5:c.336G>T	NP_003311.2:p.Arg112=