Canonical Allele Identifier: CA1926173086

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87965232_87965237delinsATAGTT , CM000672.2:g.87965232_87965237delinsATAGTT	GRCh38
NC_000010.10:g.89724989_89724994delinsATAGTT , CM000672.1:g.89724989_89724994delinsATAGTT	GRCh37
NC_000010.9:g.89714969_89714974delinsATAGTT	NCBI36
NG_007466.2:g.106794_106799delinsATAGTT , LRG_311:g.106794_106799delinsATAGTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.1120-55_1120-50delinsATAGTT	ENSP00000514759.2:n.1120-55_1120-50delinsATAGTT
ENST00000710265.1:c.*56-55_*56-50delinsATAGTT	ENSP00000518161.1:n.*56-55_*56-50delinsATAGTT
ENST00000688158.2:n.1762-55_1762-50delinsATAGTT
ENST00000688922.2:c.*857-55_*857-50delinsATAGTT	ENSP00000508742.2:n.*857-55_*857-50delinsATAGTT
ENST00000700021.1:c.982-55_982-50delinsATAGTT	ENSP00000514757.1:n.982-55_982-50delinsATAGTT
ENST00000700022.1:c.*366-55_*366-50delinsATAGTT	ENSP00000514758.1:n.*366-55_*366-50delinsATAGTT
ENST00000700023.1:n.2185-55_2185-50delinsATAGTT
ENST00000700024.1:n.2419-55_2419-50delinsATAGTT
ENST00000706954.1:c.1027-55_1027-50delinsATAGTT	ENSP00000516674.1:n.1027-55_1027-50delinsATAGTT
ENST00000706955.1:c.*1062-55_*1062-50delinsATAGTT	ENSP00000516675.1:n.*1062-55_*1062-50delinsATAGTT
ENST00000686459.1:c.*613-55_*613-50delinsATAGTT	ENSP00000508909.1:n.*613-55_*613-50delinsATAGTT
ENST00000688158.1:c.*1138-55_*1138-50delinsATAGTT	ENSP00000509254.1:n.*1138-55_*1138-50delinsATAGTT
ENST00000688308.1:c.1027-55_1027-50delinsATAGTT	ENSP00000508752.1:n.1027-55_1027-50delinsATAGTT
ENST00000688922.1:c.948-55_948-50delinsATAGTT
ENST00000693560.1:c.1546-55_1546-50delinsATAGTT	ENSP00000509861.1:n.1546-55_1546-50delinsATAGTT
ENST00000371953.8:c.1027-55_1027-50delinsATAGTT MANE Select	ENSP00000361021.3:n.1027-55_1027-50delinsATAGTT
ENST00000371953.7:c.1027-55_1027-50delinsATAGTT	ENSP00000361021.3:n.1027-55_1027-50delinsATAGTT
NM_000314.5:c.1027-55_1027-50delinsATAGTT	NP_000305.3:n.1027-55_1027-50delinsATAGTT
NM_000314.6:c.1027-55_1027-50delinsATAGTT	NP_000305.3:n.1027-55_1027-50delinsATAGTT
NM_001304717.2:c.1546-55_1546-50delinsATAGTT	NP_001291646.2:n.1546-55_1546-50delinsATAGTT
NM_001304718.1:c.436-55_436-50delinsATAGTT	NP_001291647.1:n.436-55_436-50delinsATAGTT
XM_006717926.2:c.982-55_982-50delinsATAGTT	XP_006717989.1:n.982-55_982-50delinsATAGTT
XM_011539982.1:c.931-55_931-50delinsATAGTT	XP_011538284.1:n.931-55_931-50delinsATAGTT
XR_945791.1:n.1597-55_1597-50delinsATAGTT
NM_000314.7:c.1027-55_1027-50delinsATAGTT	NP_000305.3:n.1027-55_1027-50delinsATAGTT
NM_001304717.5:c.1546-55_1546-50delinsATAGTT	NP_001291646.4:n.1546-55_1546-50delinsATAGTT
NM_001304718.2:c.436-55_436-50delinsATAGTT	NP_001291647.1:n.436-55_436-50delinsATAGTT
NM_000314.8:c.1027-55_1027-50delinsATAGTT MANE Select	NP_000305.3:n.1027-55_1027-50delinsATAGTT