Canonical Allele Identifier: CA379562731

Gene: TUB

Linked Data

• MyVariant Identifiers: chr11:g.8111665T>A (hg19) ; chr11:g.8090118T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.8090118T>A , CM000673.2:g.8090118T>A	GRCh38
NC_000011.9:g.8111665T>A , CM000673.1:g.8111665T>A	GRCh37
NC_000011.8:g.8068241T>A	NCBI36
NG_029912.1:g.56486T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299506.3:c.140T>A MANE Select	ENSP00000299506.3:p.Met47Lys
ENST00000299506.2:c.140T>A	ENSP00000299506.2:p.Met47Lys
ENST00000305253.8:c.305T>A	ENSP00000305426.4:p.Met102Lys
ENST00000534099.5:c.158T>A	ENSP00000434400.1:p.Met53Lys
NM_003320.4:c.305T>A	NP_003311.2:p.Met102Lys
NM_177972.2:c.140T>A	NP_813977.1:p.Met47Lys
XM_005253109.2:c.266T>A	XP_005253166.1:p.Met89Lys
XM_011520344.1:c.176T>A	XP_011518646.1:p.Met59Lys
XM_005253109.3:c.266T>A	XP_005253166.1:p.Met89Lys
XM_011520344.2:c.176T>A	XP_011518646.1:p.Met59Lys
NM_177972.3:c.140T>A MANE Select	NP_813977.1:p.Met47Lys
NM_003320.5:c.305T>A	NP_003311.2:p.Met102Lys