Canonical Allele Identifier: CA597322514

Gene: TUB

Linked Data

• dbSNP Id: rs1328419477
• gnomAD v2: 11-8111334-A-G
• gnomAD v3: 11-8089787-A-G
• gnomAD v4: 11-8089787-A-G
• MyVariant Identifiers: chr11:g.8111334A>G (hg19) ; chr11:g.8089787A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.8089787A>G , CM000673.2:g.8089787A>G	GRCh38
NC_000011.9:g.8111334A>G , CM000673.1:g.8111334A>G	GRCh37
NC_000011.8:g.8067910A>G	NCBI36
NG_029912.1:g.56155A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299506.3:c.90+126A>G MANE Select	ENSP00000299506.3:n.90+126A>G
ENST00000299506.2:c.90+126A>G	ENSP00000299506.2:n.90+126A>G
ENST00000305253.8:c.255+126A>G	ENSP00000305426.4:n.255+126A>G
ENST00000534099.5:c.108+126A>G	ENSP00000434400.1:n.108+126A>G
NM_003320.4:c.255+126A>G	NP_003311.2:n.255+126A>G
NM_177972.2:c.90+126A>G	NP_813977.1:n.90+126A>G
XM_005253109.2:c.216+126A>G	XP_005253166.1:n.216+126A>G
XM_011520344.1:c.126+126A>G	XP_011518646.1:n.126+126A>G
XM_005253109.3:c.216+126A>G	XP_005253166.1:n.216+126A>G
XM_011520344.2:c.126+126A>G	XP_011518646.1:n.126+126A>G
NM_177972.3:c.90+126A>G MANE Select	NP_813977.1:n.90+126A>G
NM_003320.5:c.255+126A>G	NP_003311.2:n.255+126A>G