Canonical Allele Identifier: CA379562955

Gene: TUB

Linked Data

• MyVariant Identifiers: chr11:g.8111719A>T (hg19) ; chr11:g.8090172A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.8090172A>T , CM000673.2:g.8090172A>T	GRCh38
NC_000011.9:g.8111719A>T , CM000673.1:g.8111719A>T	GRCh37
NC_000011.8:g.8068295A>T	NCBI36
NG_029912.1:g.56540A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299506.3:c.194A>T MANE Select	ENSP00000299506.3:p.Glu65Val
ENST00000299506.2:c.194A>T	ENSP00000299506.2:p.Glu65Val
ENST00000305253.8:c.359A>T	ENSP00000305426.4:p.Glu120Val
ENST00000534099.5:c.212A>T	ENSP00000434400.1:p.Glu71Val
NM_003320.4:c.359A>T	NP_003311.2:p.Glu120Val
NM_177972.2:c.194A>T	NP_813977.1:p.Glu65Val
XM_005253109.2:c.320A>T	XP_005253166.1:p.Glu107Val
XM_011520344.1:c.230A>T	XP_011518646.1:p.Glu77Val
XM_005253109.3:c.320A>T	XP_005253166.1:p.Glu107Val
XM_011520344.2:c.230A>T	XP_011518646.1:p.Glu77Val
NM_177972.3:c.194A>T MANE Select	NP_813977.1:p.Glu65Val
NM_003320.5:c.359A>T	NP_003311.2:p.Glu120Val