Canonical Allele Identifier: CA379562584

Gene: TUB

Linked Data

• MyVariant Identifiers: chr11:g.8111629A>T (hg19) ; chr11:g.8090082A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.8090082A>T , CM000673.2:g.8090082A>T	GRCh38
NC_000011.9:g.8111629A>T , CM000673.1:g.8111629A>T	GRCh37
NC_000011.8:g.8068205A>T	NCBI36
NG_029912.1:g.56450A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299506.3:c.104A>T MANE Select	ENSP00000299506.3:p.Glu35Val
ENST00000299506.2:c.104A>T	ENSP00000299506.2:p.Glu35Val
ENST00000305253.8:c.269A>T	ENSP00000305426.4:p.Glu90Val
ENST00000534099.5:c.122A>T	ENSP00000434400.1:p.Glu41Val
NM_003320.4:c.269A>T	NP_003311.2:p.Glu90Val
NM_177972.2:c.104A>T	NP_813977.1:p.Glu35Val
XM_005253109.2:c.230A>T	XP_005253166.1:p.Glu77Val
XM_011520344.1:c.140A>T	XP_011518646.1:p.Glu47Val
XM_005253109.3:c.230A>T	XP_005253166.1:p.Glu77Val
XM_011520344.2:c.140A>T	XP_011518646.1:p.Glu47Val
NM_177972.3:c.104A>T MANE Select	NP_813977.1:p.Glu35Val
NM_003320.5:c.269A>T	NP_003311.2:p.Glu90Val