Canonical Allele Identifier: CA379562735

Gene: TUB

Linked Data

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

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299506.3:c.140T>G MANE Select	ENSP00000299506.3:p.Met47Arg
ENST00000299506.2:c.140T>G	ENSP00000299506.2:p.Met47Arg
ENST00000305253.8:c.305T>G	ENSP00000305426.4:p.Met102Arg
ENST00000534099.5:c.158T>G	ENSP00000434400.1:p.Met53Arg
NM_003320.4:c.305T>G	NP_003311.2:p.Met102Arg
NM_177972.2:c.140T>G	NP_813977.1:p.Met47Arg
XM_005253109.2:c.266T>G	XP_005253166.1:p.Met89Arg
XM_011520344.1:c.176T>G	XP_011518646.1:p.Met59Arg
XM_005253109.3:c.266T>G	XP_005253166.1:p.Met89Arg
XM_011520344.2:c.176T>G	XP_011518646.1:p.Met59Arg
NM_177972.3:c.140T>G MANE Select	NP_813977.1:p.Met47Arg
NM_003320.5:c.305T>G	NP_003311.2:p.Met102Arg