Canonical Allele Identifier: CA1926173033

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87965201_87965204delinsTAAA , CM000672.2:g.87965201_87965204delinsTAAA	GRCh38
NC_000010.10:g.89724958_89724961delinsTAAA , CM000672.1:g.89724958_89724961delinsTAAA	GRCh37
NC_000010.9:g.89714938_89714941delinsTAAA	NCBI36
NG_007466.2:g.106763_106766delinsTAAA , LRG_311:g.106763_106766delinsTAAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.1120-86_1120-83delinsTAAA	ENSP00000514759.2:n.1120-86_1120-83delinsTAAA
ENST00000710265.1:c.*56-86_*56-83delinsTAAA	ENSP00000518161.1:n.*56-86_*56-83delinsTAAA
ENST00000688158.2:n.1762-86_1762-83delinsTAAA
ENST00000688922.2:c.*857-86_*857-83delinsTAAA	ENSP00000508742.2:n.*857-86_*857-83delinsTAAA
ENST00000700021.1:c.982-86_982-83delinsTAAA	ENSP00000514757.1:n.982-86_982-83delinsTAAA
ENST00000700022.1:c.*366-86_*366-83delinsTAAA	ENSP00000514758.1:n.*366-86_*366-83delinsTAAA
ENST00000700023.1:n.2185-86_2185-83delinsTAAA
ENST00000700024.1:n.2419-86_2419-83delinsTAAA
ENST00000706954.1:c.1027-86_1027-83delinsTAAA	ENSP00000516674.1:n.1027-86_1027-83delinsTAAA
ENST00000706955.1:c.*1062-86_*1062-83delinsTAAA	ENSP00000516675.1:n.*1062-86_*1062-83delinsTAAA
ENST00000686459.1:c.*613-86_*613-83delinsTAAA	ENSP00000508909.1:n.*613-86_*613-83delinsTAAA
ENST00000688158.1:c.*1138-86_*1138-83delinsTAAA	ENSP00000509254.1:n.*1138-86_*1138-83delinsTAAA
ENST00000688308.1:c.1027-86_1027-83delinsTAAA	ENSP00000508752.1:n.1027-86_1027-83delinsTAAA
ENST00000688922.1:c.948-86_948-83delinsTAAA
ENST00000693560.1:c.1546-86_1546-83delinsTAAA	ENSP00000509861.1:n.1546-86_1546-83delinsTAAA
ENST00000371953.8:c.1027-86_1027-83delinsTAAA MANE Select	ENSP00000361021.3:n.1027-86_1027-83delinsTAAA
ENST00000371953.7:c.1027-86_1027-83delinsTAAA	ENSP00000361021.3:n.1027-86_1027-83delinsTAAA
NM_000314.5:c.1027-86_1027-83delinsTAAA	NP_000305.3:n.1027-86_1027-83delinsTAAA
NM_000314.6:c.1027-86_1027-83delinsTAAA	NP_000305.3:n.1027-86_1027-83delinsTAAA
NM_001304717.2:c.1546-86_1546-83delinsTAAA	NP_001291646.2:n.1546-86_1546-83delinsTAAA
NM_001304718.1:c.436-86_436-83delinsTAAA	NP_001291647.1:n.436-86_436-83delinsTAAA
XM_006717926.2:c.982-86_982-83delinsTAAA	XP_006717989.1:n.982-86_982-83delinsTAAA
XM_011539982.1:c.931-86_931-83delinsTAAA	XP_011538284.1:n.931-86_931-83delinsTAAA
XR_945791.1:n.1597-86_1597-83delinsTAAA
NM_000314.7:c.1027-86_1027-83delinsTAAA	NP_000305.3:n.1027-86_1027-83delinsTAAA
NM_001304717.5:c.1546-86_1546-83delinsTAAA	NP_001291646.4:n.1546-86_1546-83delinsTAAA
NM_001304718.2:c.436-86_436-83delinsTAAA	NP_001291647.1:n.436-86_436-83delinsTAAA
NM_000314.8:c.1027-86_1027-83delinsTAAA MANE Select	NP_000305.3:n.1027-86_1027-83delinsTAAA