Canonical Allele Identifier: CA379562694

Gene: TUB

Linked Data

• MyVariant Identifiers: chr11:g.8111656A>T (hg19) ; chr11:g.8090109A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.8090109A>T , CM000673.2:g.8090109A>T	GRCh38
NC_000011.9:g.8111656A>T , CM000673.1:g.8111656A>T	GRCh37
NC_000011.8:g.8068232A>T	NCBI36
NG_029912.1:g.56477A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299506.3:c.131A>T MANE Select	ENSP00000299506.3:p.Glu44Val
ENST00000299506.2:c.131A>T	ENSP00000299506.2:p.Glu44Val
ENST00000305253.8:c.296A>T	ENSP00000305426.4:p.Glu99Val
ENST00000534099.5:c.149A>T	ENSP00000434400.1:p.Glu50Val
NM_003320.4:c.296A>T	NP_003311.2:p.Glu99Val
NM_177972.2:c.131A>T	NP_813977.1:p.Glu44Val
XM_005253109.2:c.257A>T	XP_005253166.1:p.Glu86Val
XM_011520344.1:c.167A>T	XP_011518646.1:p.Glu56Val
XM_005253109.3:c.257A>T	XP_005253166.1:p.Glu86Val
XM_011520344.2:c.167A>T	XP_011518646.1:p.Glu56Val
NM_177972.3:c.131A>T MANE Select	NP_813977.1:p.Glu44Val
NM_003320.5:c.296A>T	NP_003311.2:p.Glu99Val