Canonical Allele Identifier: CA891838075

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87965431_87965432delinsAT , CM000672.2:g.87965431_87965432delinsAT	GRCh38
NC_000010.10:g.89725188_89725189delinsAT , CM000672.1:g.89725188_89725189delinsAT	GRCh37
NC_000010.9:g.89715168_89715169delinsAT	NCBI36
NG_007466.2:g.106993_106994delinsAT , LRG_311:g.106993_106994delinsAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.1264_1265delinsAT	ENSP00000514759.2:p.Pro422Ile
ENST00000710265.1:c.*200_*201delinsAT	ENSP00000518161.1:n.*200_*201delinsAT
ENST00000688158.2:n.1906_1907delinsAT
ENST00000688922.2:c.*1001_*1002delinsAT	ENSP00000508742.2:n.*1001_*1002delinsAT
ENST00000700021.1:c.1126_1127delinsAT	ENSP00000514757.1:p.Pro376Ile
ENST00000700022.1:c.*510_*511delinsAT	ENSP00000514758.1:n.*510_*511delinsAT
ENST00000700023.1:n.2329_2330delinsAT
ENST00000700024.1:n.2563_2564delinsAT
ENST00000706954.1:c.1171_1172delinsAT	ENSP00000516674.1:p.Pro391Ile
ENST00000706955.1:c.*1206_*1207delinsAT	ENSP00000516675.1:n.*1206_*1207delinsAT
ENST00000686459.1:c.*757_*758delinsAT	ENSP00000508909.1:n.*757_*758delinsAT
ENST00000688158.1:c.*1282_*1283delinsAT	ENSP00000509254.1:n.*1282_*1283delinsAT
ENST00000688308.1:c.1171_1172delinsAT	ENSP00000508752.1:p.Pro391Ile
ENST00000688922.1:c.1092_1093delinsAT
ENST00000693560.1:c.1690_1691delinsAT	ENSP00000509861.1:p.Pro564Ile
ENST00000371953.8:c.1171_1172delinsAT MANE Select	ENSP00000361021.3:p.Pro391Ile
ENST00000371953.7:c.1171_1172delinsAT	ENSP00000361021.3:p.Pro391Ile
NM_000314.5:c.1171_1172delinsAT	NP_000305.3:p.Pro391Ile
NM_000314.6:c.1171_1172delinsAT	NP_000305.3:p.Pro391Ile
NM_001304717.2:c.1690_1691delinsAT	NP_001291646.2:p.Pro564Ile
NM_001304718.1:c.580_581delinsAT	NP_001291647.1:p.Pro194Ile
XM_006717926.2:c.1126_1127delinsAT	XP_006717989.1:p.Pro376Ile
XM_011539982.1:c.1075_1076delinsAT	XP_011538284.1:p.Pro359Ile
XR_945791.1:n.1741_1742delinsAT
NM_000314.7:c.1171_1172delinsAT	NP_000305.3:p.Pro391Ile
NM_001304717.5:c.1690_1691delinsAT	NP_001291646.4:p.Pro564Ile
NM_001304718.2:c.580_581delinsAT	NP_001291647.1:p.Pro194Ile
NM_000314.8:c.1171_1172delinsAT MANE Select	NP_000305.3:p.Pro391Ile