Canonical Allele Identifier: CA5870934

Gene: TUB

Linked Data

• dbSNP Id: rs577358762
• ExAC: 11:8111190 G / A
• gnomAD v2: 11-8111190-G-A
• gnomAD v3: 11-8089643-G-A
• gnomAD v4: 11-8089643-G-A
• MyVariant Identifiers: chr11:g.8111190G>A (hg19) ; chr11:g.8089643G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.8089643G>A , CM000673.2:g.8089643G>A	GRCh38
NC_000011.9:g.8111190G>A , CM000673.1:g.8111190G>A	GRCh37
NC_000011.8:g.8067766G>A	NCBI36
NG_029912.1:g.56011G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299506.3:c.72G>A MANE Select	ENSP00000299506.3:p.Gln24=
ENST00000299506.2:c.72G>A	ENSP00000299506.2:p.Gln24=
ENST00000305253.8:c.237G>A	ENSP00000305426.4:p.Gln79=
ENST00000534099.5:c.90G>A	ENSP00000434400.1:p.Gln30=
NM_003320.4:c.237G>A	NP_003311.2:p.Gln79=
NM_177972.2:c.72G>A	NP_813977.1:p.Gln24=
XM_005253109.2:c.198G>A	XP_005253166.1:p.Gln66=
XM_011520344.1:c.108G>A	XP_011518646.1:p.Gln36=
XM_005253109.3:c.198G>A	XP_005253166.1:p.Gln66=
XM_011520344.2:c.108G>A	XP_011518646.1:p.Gln36=
NM_177972.3:c.72G>A MANE Select	NP_813977.1:p.Gln24=
NM_003320.5:c.237G>A	NP_003311.2:p.Gln79=