Canonical Allele Identifier: CA1926172861

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87965040_87965044delinsAAAAT , CM000672.2:g.87965040_87965044delinsAAAAT	GRCh38
NC_000010.10:g.89724797_89724801delinsAAAAT , CM000672.1:g.89724797_89724801delinsAAAAT	GRCh37
NC_000010.9:g.89714777_89714781delinsAAAAT	NCBI36
NG_007466.2:g.106602_106606delinsAAAAT , LRG_311:g.106602_106606delinsAAAAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.1120-247_1120-243delinsAAAAT	ENSP00000514759.2:n.1120-247_1120-243delinsAAAAT
ENST00000710265.1:c.*56-247_*56-243delinsAAAAT	ENSP00000518161.1:n.*56-247_*56-243delinsAAAAT
ENST00000688158.2:n.1762-247_1762-243delinsAAAAT
ENST00000688922.2:c.*857-247_*857-243delinsAAAAT	ENSP00000508742.2:n.*857-247_*857-243delinsAAAAT
ENST00000700021.1:c.982-247_982-243delinsAAAAT	ENSP00000514757.1:n.982-247_982-243delinsAAAAT
ENST00000700022.1:c.*366-247_*366-243delinsAAAAT	ENSP00000514758.1:n.*366-247_*366-243delinsAAAAT
ENST00000700023.1:n.2185-247_2185-243delinsAAAAT
ENST00000700024.1:n.2419-247_2419-243delinsAAAAT
ENST00000706954.1:c.1027-247_1027-243delinsAAAAT	ENSP00000516674.1:n.1027-247_1027-243delinsAAAAT
ENST00000706955.1:c.*1062-247_*1062-243delinsAAAAT	ENSP00000516675.1:n.*1062-247_*1062-243delinsAAAAT
ENST00000686459.1:c.*613-247_*613-243delinsAAAAT	ENSP00000508909.1:n.*613-247_*613-243delinsAAAAT
ENST00000688158.1:c.*1138-247_*1138-243delinsAAAAT	ENSP00000509254.1:n.*1138-247_*1138-243delinsAAAAT
ENST00000688308.1:c.1027-247_1027-243delinsAAAAT	ENSP00000508752.1:n.1027-247_1027-243delinsAAAAT
ENST00000688922.1:c.948-247_948-243delinsAAAAT
ENST00000693560.1:c.1546-247_1546-243delinsAAAAT	ENSP00000509861.1:n.1546-247_1546-243delinsAAAAT
ENST00000371953.8:c.1027-247_1027-243delinsAAAAT MANE Select	ENSP00000361021.3:n.1027-247_1027-243delinsAAAAT
ENST00000371953.7:c.1027-247_1027-243delinsAAAAT	ENSP00000361021.3:n.1027-247_1027-243delinsAAAAT
NM_000314.5:c.1027-247_1027-243delinsAAAAT	NP_000305.3:n.1027-247_1027-243delinsAAAAT
NM_000314.6:c.1027-247_1027-243delinsAAAAT	NP_000305.3:n.1027-247_1027-243delinsAAAAT
NM_001304717.2:c.1546-247_1546-243delinsAAAAT	NP_001291646.2:n.1546-247_1546-243delinsAAAAT
NM_001304718.1:c.436-247_436-243delinsAAAAT	NP_001291647.1:n.436-247_436-243delinsAAAAT
XM_006717926.2:c.982-247_982-243delinsAAAAT	XP_006717989.1:n.982-247_982-243delinsAAAAT
XM_011539982.1:c.931-247_931-243delinsAAAAT	XP_011538284.1:n.931-247_931-243delinsAAAAT
XR_945791.1:n.1597-247_1597-243delinsAAAAT
NM_000314.7:c.1027-247_1027-243delinsAAAAT	NP_000305.3:n.1027-247_1027-243delinsAAAAT
NM_001304717.5:c.1546-247_1546-243delinsAAAAT	NP_001291646.4:n.1546-247_1546-243delinsAAAAT
NM_001304718.2:c.436-247_436-243delinsAAAAT	NP_001291647.1:n.436-247_436-243delinsAAAAT
NM_000314.8:c.1027-247_1027-243delinsAAAAT MANE Select	NP_000305.3:n.1027-247_1027-243delinsAAAAT