Canonical Allele Identifier: CA2579926667

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87965326_87965328del , CM000672.2:g.87965326_87965328del	GRCh38
NC_000010.10:g.89725083_89725085del , CM000672.1:g.89725083_89725085del	GRCh37
NC_000010.9:g.89715063_89715065del	NCBI36
NG_007466.2:g.106888_106890del , LRG_311:g.106888_106890del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.1159_1161del	ENSP00000514759.2:p.Asn387del
ENST00000710265.1:c.*95_*97del	ENSP00000518161.1:n.*95_*97del
ENST00000688158.2:n.1801_1803del
ENST00000688922.2:c.*896_*898del	ENSP00000508742.2:n.*896_*898del
ENST00000700021.1:c.1021_1023del	ENSP00000514757.1:p.Asn341del
ENST00000700022.1:c.*405_*407del	ENSP00000514758.1:n.*405_*407del
ENST00000700023.1:n.2224_2226del
ENST00000700024.1:n.2458_2460del
ENST00000706954.1:c.1066_1068del	ENSP00000516674.1:p.Asn356del
ENST00000706955.1:c.*1101_*1103del	ENSP00000516675.1:n.*1101_*1103del
ENST00000686459.1:c.*652_*654del	ENSP00000508909.1:n.*652_*654del
ENST00000688158.1:c.*1177_*1179del	ENSP00000509254.1:n.*1177_*1179del
ENST00000688308.1:c.1066_1068del	ENSP00000508752.1:p.Asn356del
ENST00000688922.1:c.987_989del
ENST00000693560.1:c.1585_1587del	ENSP00000509861.1:p.Asn529del
ENST00000371953.8:c.1066_1068del MANE Select	ENSP00000361021.3:p.Asn356del
ENST00000371953.7:c.1066_1068del	ENSP00000361021.3:p.Asn356del
NM_000314.5:c.1066_1068del	NP_000305.3:p.Asn356del
NM_000314.6:c.1066_1068del	NP_000305.3:p.Asn356del
NM_001304717.2:c.1585_1587del	NP_001291646.2:p.Asn529del
NM_001304718.1:c.475_477del	NP_001291647.1:p.Asn159del
XM_006717926.2:c.1021_1023del	XP_006717989.1:p.Asn341del
XM_011539982.1:c.970_972del	XP_011538284.1:p.Asn324del
XR_945791.1:n.1636_1638del
NM_000314.7:c.1066_1068del	NP_000305.3:p.Asn356del
NM_001304717.5:c.1585_1587del	NP_001291646.4:p.Asn529del
NM_001304718.2:c.475_477del	NP_001291647.1:p.Asn159del
NM_000314.8:c.1066_1068del MANE Select	NP_000305.3:p.Asn356del