Canonical Allele Identifier: CA891838073

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87965431_87965433delinsTGG , CM000672.2:g.87965431_87965433delinsTGG	GRCh38
NC_000010.10:g.89725188_89725190delinsTGG , CM000672.1:g.89725188_89725190delinsTGG	GRCh37
NC_000010.9:g.89715168_89715170delinsTGG	NCBI36
NG_007466.2:g.106993_106995delinsTGG , LRG_311:g.106993_106995delinsTGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.1264_1266delinsTGG	ENSP00000514759.2:p.Pro422Trp
ENST00000710265.1:c.*200_*202delinsTGG	ENSP00000518161.1:n.*200_*202delinsTGG
ENST00000688158.2:n.1906_1908delinsTGG
ENST00000688922.2:c.*1001_*1003delinsTGG	ENSP00000508742.2:n.*1001_*1003delinsTGG
ENST00000700021.1:c.1126_1128delinsTGG	ENSP00000514757.1:p.Pro376Trp
ENST00000700022.1:c.*510_*512delinsTGG	ENSP00000514758.1:n.*510_*512delinsTGG
ENST00000700023.1:n.2329_2331delinsTGG
ENST00000700024.1:n.2563_2565delinsTGG
ENST00000706954.1:c.1171_1173delinsTGG	ENSP00000516674.1:p.Pro391Trp
ENST00000706955.1:c.*1206_*1208delinsTGG	ENSP00000516675.1:n.*1206_*1208delinsTGG
ENST00000686459.1:c.*757_*759delinsTGG	ENSP00000508909.1:n.*757_*759delinsTGG
ENST00000688158.1:c.*1282_*1284delinsTGG	ENSP00000509254.1:n.*1282_*1284delinsTGG
ENST00000688308.1:c.1171_1173delinsTGG	ENSP00000508752.1:p.Pro391Trp
ENST00000688922.1:c.1092_1094delinsTGG
ENST00000693560.1:c.1690_1692delinsTGG	ENSP00000509861.1:p.Pro564Trp
ENST00000371953.8:c.1171_1173delinsTGG MANE Select	ENSP00000361021.3:p.Pro391Trp
ENST00000371953.7:c.1171_1173delinsTGG	ENSP00000361021.3:p.Pro391Trp
NM_000314.5:c.1171_1173delinsTGG	NP_000305.3:p.Pro391Trp
NM_000314.6:c.1171_1173delinsTGG	NP_000305.3:p.Pro391Trp
NM_001304717.2:c.1690_1692delinsTGG	NP_001291646.2:p.Pro564Trp
NM_001304718.1:c.580_582delinsTGG	NP_001291647.1:p.Pro194Trp
XM_006717926.2:c.1126_1128delinsTGG	XP_006717989.1:p.Pro376Trp
XM_011539982.1:c.1075_1077delinsTGG	XP_011538284.1:p.Pro359Trp
XR_945791.1:n.1741_1743delinsTGG
NM_000314.7:c.1171_1173delinsTGG	NP_000305.3:p.Pro391Trp
NM_001304717.5:c.1690_1692delinsTGG	NP_001291646.4:p.Pro564Trp
NM_001304718.2:c.580_582delinsTGG	NP_001291647.1:p.Pro194Trp
NM_000314.8:c.1171_1173delinsTGG MANE Select	NP_000305.3:p.Pro391Trp