Canonical Allele Identifier: CA379562308

Gene: TUB

Linked Data

• gnomAD v4: 11-8089627-G-A
• MyVariant Identifiers: chr11:g.8111174G>A (hg19) ; chr11:g.8089627G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.8089627G>A , CM000673.2:g.8089627G>A	GRCh38
NC_000011.9:g.8111174G>A , CM000673.1:g.8111174G>A	GRCh37
NC_000011.8:g.8067750G>A	NCBI36
NG_029912.1:g.55995G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299506.3:c.56G>A MANE Select	ENSP00000299506.3:p.Gly19Asp
ENST00000299506.2:c.56G>A	ENSP00000299506.2:p.Gly19Asp
ENST00000305253.8:c.221G>A	ENSP00000305426.4:p.Gly74Asp
ENST00000534099.5:c.74G>A	ENSP00000434400.1:p.Gly25Asp
NM_003320.4:c.221G>A	NP_003311.2:p.Gly74Asp
NM_177972.2:c.56G>A	NP_813977.1:p.Gly19Asp
XM_005253109.2:c.182G>A	XP_005253166.1:p.Gly61Asp
XM_011520344.1:c.92G>A	XP_011518646.1:p.Gly31Asp
XM_005253109.3:c.182G>A	XP_005253166.1:p.Gly61Asp
XM_011520344.2:c.92G>A	XP_011518646.1:p.Gly31Asp
NM_177972.3:c.56G>A MANE Select	NP_813977.1:p.Gly19Asp
NM_003320.5:c.221G>A	NP_003311.2:p.Gly74Asp