Canonical Allele Identifier: CA2579986011

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87965431_87965433del , CM000672.2:g.87965431_87965433del	GRCh38
NC_000010.10:g.89725188_89725190del , CM000672.1:g.89725188_89725190del	GRCh37
NC_000010.9:g.89715168_89715170del	NCBI36
NG_007466.2:g.106993_106995del , LRG_311:g.106993_106995del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.1264_1266del	ENSP00000514759.2:p.Pro422del
ENST00000710265.1:c.*200_*202del	ENSP00000518161.1:n.*200_*202del
ENST00000688158.2:n.1906_1908del
ENST00000688922.2:c.*1001_*1003del	ENSP00000508742.2:n.*1001_*1003del
ENST00000700021.1:c.1126_1128del	ENSP00000514757.1:p.Pro376del
ENST00000700022.1:c.*510_*512del	ENSP00000514758.1:n.*510_*512del
ENST00000700023.1:n.2329_2331del
ENST00000700024.1:n.2563_2565del
ENST00000706954.1:c.1171_1173del	ENSP00000516674.1:p.Pro391del
ENST00000706955.1:c.*1206_*1208del	ENSP00000516675.1:n.*1206_*1208del
ENST00000686459.1:c.*757_*759del	ENSP00000508909.1:n.*757_*759del
ENST00000688158.1:c.*1282_*1284del	ENSP00000509254.1:n.*1282_*1284del
ENST00000688308.1:c.1171_1173del	ENSP00000508752.1:p.Pro391del
ENST00000688922.1:c.1092_1094del
ENST00000693560.1:c.1690_1692del	ENSP00000509861.1:p.Pro564del
ENST00000371953.8:c.1171_1173del MANE Select	ENSP00000361021.3:p.Pro391del
ENST00000371953.7:c.1171_1173del	ENSP00000361021.3:p.Pro391del
NM_000314.5:c.1171_1173del	NP_000305.3:p.Pro391del
NM_000314.6:c.1171_1173del	NP_000305.3:p.Pro391del
NM_001304717.2:c.1690_1692del	NP_001291646.2:p.Pro564del
NM_001304718.1:c.580_582del	NP_001291647.1:p.Pro194del
XM_006717926.2:c.1126_1128del	XP_006717989.1:p.Pro376del
XM_011539982.1:c.1075_1077del	XP_011538284.1:p.Pro359del
XR_945791.1:n.1741_1743del
NM_000314.7:c.1171_1173del	NP_000305.3:p.Pro391del
NM_001304717.5:c.1690_1692del	NP_001291646.4:p.Pro564del
NM_001304718.2:c.580_582del	NP_001291647.1:p.Pro194del
NM_000314.8:c.1171_1173del MANE Select	NP_000305.3:p.Pro391del