Canonical Allele Identifier: CA379562562

Gene: TUB

Linked Data

• MyVariant Identifiers: chr11:g.8111625C>G (hg19) ; chr11:g.8090078C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.8090078C>G , CM000673.2:g.8090078C>G	GRCh38
NC_000011.9:g.8111625C>G , CM000673.1:g.8111625C>G	GRCh37
NC_000011.8:g.8068201C>G	NCBI36
NG_029912.1:g.56446C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299506.3:c.100C>G MANE Select	ENSP00000299506.3:p.Leu34Val
ENST00000299506.2:c.100C>G	ENSP00000299506.2:p.Leu34Val
ENST00000305253.8:c.265C>G	ENSP00000305426.4:p.Leu89Val
ENST00000534099.5:c.118C>G	ENSP00000434400.1:p.Leu40Val
NM_003320.4:c.265C>G	NP_003311.2:p.Leu89Val
NM_177972.2:c.100C>G	NP_813977.1:p.Leu34Val
XM_005253109.2:c.226C>G	XP_005253166.1:p.Leu76Val
XM_011520344.1:c.136C>G	XP_011518646.1:p.Leu46Val
XM_005253109.3:c.226C>G	XP_005253166.1:p.Leu76Val
XM_011520344.2:c.136C>G	XP_011518646.1:p.Leu46Val
NM_177972.3:c.100C>G MANE Select	NP_813977.1:p.Leu34Val
NM_003320.5:c.265C>G	NP_003311.2:p.Leu89Val