Canonical Allele Identifier: CA2610049164

Gene: PTEN

Linked Data

• gnomAD v4: 10-87965217-A-AT

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87965217_87965218insT , CM000672.2:g.87965217_87965218insT	GRCh38
NC_000010.10:g.89724974_89724975insT , CM000672.1:g.89724974_89724975insT	GRCh37
NC_000010.9:g.89714954_89714955insT	NCBI36
NG_007466.2:g.106779_106780insT , LRG_311:g.106779_106780insT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.1120-70_1120-69insT	ENSP00000514759.2:n.1120-70_1120-69insT
ENST00000710265.1:c.*56-70_*56-69insT	ENSP00000518161.1:n.*56-70_*56-69insT
ENST00000688158.2:n.1762-70_1762-69insT
ENST00000688922.2:c.*857-70_*857-69insT	ENSP00000508742.2:n.*857-70_*857-69insT
ENST00000700021.1:c.982-70_982-69insT	ENSP00000514757.1:n.982-70_982-69insT
ENST00000700022.1:c.*366-70_*366-69insT	ENSP00000514758.1:n.*366-70_*366-69insT
ENST00000700023.1:n.2185-70_2185-69insT
ENST00000700024.1:n.2419-70_2419-69insT
ENST00000706954.1:c.1027-70_1027-69insT	ENSP00000516674.1:n.1027-70_1027-69insT
ENST00000706955.1:c.*1062-70_*1062-69insT	ENSP00000516675.1:n.*1062-70_*1062-69insT
ENST00000686459.1:c.*613-70_*613-69insT	ENSP00000508909.1:n.*613-70_*613-69insT
ENST00000688158.1:c.*1138-70_*1138-69insT	ENSP00000509254.1:n.*1138-70_*1138-69insT
ENST00000688308.1:c.1027-70_1027-69insT	ENSP00000508752.1:n.1027-70_1027-69insT
ENST00000688922.1:c.948-70_948-69insT
ENST00000693560.1:c.1546-70_1546-69insT	ENSP00000509861.1:n.1546-70_1546-69insT
ENST00000371953.8:c.1027-70_1027-69insT MANE Select	ENSP00000361021.3:n.1027-70_1027-69insT
ENST00000371953.7:c.1027-70_1027-69insT	ENSP00000361021.3:n.1027-70_1027-69insT
NM_000314.5:c.1027-70_1027-69insT	NP_000305.3:n.1027-70_1027-69insT
NM_000314.6:c.1027-70_1027-69insT	NP_000305.3:n.1027-70_1027-69insT
NM_001304717.2:c.1546-70_1546-69insT	NP_001291646.2:n.1546-70_1546-69insT
NM_001304718.1:c.436-70_436-69insT	NP_001291647.1:n.436-70_436-69insT
XM_006717926.2:c.982-70_982-69insT	XP_006717989.1:n.982-70_982-69insT
XM_011539982.1:c.931-70_931-69insT	XP_011538284.1:n.931-70_931-69insT
XR_945791.1:n.1597-70_1597-69insT
NM_000314.7:c.1027-70_1027-69insT	NP_000305.3:n.1027-70_1027-69insT
NM_001304717.5:c.1546-70_1546-69insT	NP_001291646.4:n.1546-70_1546-69insT
NM_001304718.2:c.436-70_436-69insT	NP_001291647.1:n.436-70_436-69insT
NM_000314.8:c.1027-70_1027-69insT MANE Select	NP_000305.3:n.1027-70_1027-69insT