Canonical Allele Identifier: CA379562566

Gene: TUB

Linked Data

• MyVariant Identifiers: chr11:g.8111626T>A (hg19) ; chr11:g.8090079T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.8090079T>A , CM000673.2:g.8090079T>A	GRCh38
NC_000011.9:g.8111626T>A , CM000673.1:g.8111626T>A	GRCh37
NC_000011.8:g.8068202T>A	NCBI36
NG_029912.1:g.56447T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299506.3:c.101T>A MANE Select	ENSP00000299506.3:p.Leu34Gln
ENST00000299506.2:c.101T>A	ENSP00000299506.2:p.Leu34Gln
ENST00000305253.8:c.266T>A	ENSP00000305426.4:p.Leu89Gln
ENST00000534099.5:c.119T>A	ENSP00000434400.1:p.Leu40Gln
NM_003320.4:c.266T>A	NP_003311.2:p.Leu89Gln
NM_177972.2:c.101T>A	NP_813977.1:p.Leu34Gln
XM_005253109.2:c.227T>A	XP_005253166.1:p.Leu76Gln
XM_011520344.1:c.137T>A	XP_011518646.1:p.Leu46Gln
XM_005253109.3:c.227T>A	XP_005253166.1:p.Leu76Gln
XM_011520344.2:c.137T>A	XP_011518646.1:p.Leu46Gln
NM_177972.3:c.101T>A MANE Select	NP_813977.1:p.Leu34Gln
NM_003320.5:c.266T>A	NP_003311.2:p.Leu89Gln