Canonical Allele Identifier: CA217414799

Gene: TUB

Linked Data

• dbSNP Id: rs1010482161
• gnomAD v2: 11-8110936-G-A
• gnomAD v3: 11-8089389-G-A
• gnomAD v4: 11-8089389-G-A
• MyVariant Identifiers: chr11:g.8110936G>A (hg19) ; chr11:g.8089389G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.8089389G>A , CM000673.2:g.8089389G>A	GRCh38
NC_000011.9:g.8110936G>A , CM000673.1:g.8110936G>A	GRCh37
NC_000011.8:g.8067512G>A	NCBI36
NG_029912.1:g.55757G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299506.3:c.39-221G>A MANE Select	ENSP00000299506.3:n.39-221G>A
ENST00000299506.2:c.39-221G>A	ENSP00000299506.2:n.39-221G>A
ENST00000305253.8:c.204-221G>A	ENSP00000305426.4:n.204-221G>A
ENST00000534099.5:c.57-221G>A	ENSP00000434400.1:n.57-221G>A
NM_003320.4:c.204-221G>A	NP_003311.2:n.204-221G>A
NM_177972.2:c.39-221G>A	NP_813977.1:n.39-221G>A
XM_005253109.2:c.165-221G>A	XP_005253166.1:n.165-221G>A
XM_011520344.1:c.75-221G>A	XP_011518646.1:n.75-221G>A
XM_005253109.3:c.165-221G>A	XP_005253166.1:n.165-221G>A
XM_011520344.2:c.75-221G>A	XP_011518646.1:n.75-221G>A
NM_177972.3:c.39-221G>A MANE Select	NP_813977.1:n.39-221G>A
NM_003320.5:c.204-221G>A	NP_003311.2:n.204-221G>A