Canonical Allele Identifier: CA2695203425

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87960915_87960932del , CM000672.2:g.87960915_87960932del	GRCh38
NC_000010.10:g.89720672_89720689del , CM000672.1:g.89720672_89720689del	GRCh37
NC_000010.9:g.89710652_89710669del	NCBI36
NG_007466.2:g.102477_102494del , LRG_311:g.102477_102494del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.916_933del	ENSP00000514759.2:p.Val306_Ile311del
ENST00000710265.1:c.823_840del	ENSP00000518161.1:p.Val275_Ile280del
ENST00000472832.3:c.823_840del	ENSP00000483066.2:p.Val275_Ile280del
ENST00000688158.2:n.1558_1575del
ENST00000688922.2:c.*653_*670del	ENSP00000508742.2:n.*653_*670del
ENST00000700021.1:c.778_795del	ENSP00000514757.1:p.Val260_Ile265del
ENST00000700022.1:c.*162_*179del	ENSP00000514758.1:n.*162_*179del
ENST00000700023.1:n.1981_1998del
ENST00000700024.1:n.2215_2232del
ENST00000700025.1:n.1592_1609del
ENST00000700026.1:n.460_477del
ENST00000700029.1:c.750_767del
ENST00000706954.1:c.823_840del	ENSP00000516674.1:p.Val275_Ile280del
ENST00000706955.1:c.*858_*875del	ENSP00000516675.1:n.*858_*875del
ENST00000686459.1:c.*409_*426del	ENSP00000508909.1:n.*409_*426del
ENST00000688158.1:c.*934_*951del	ENSP00000509254.1:n.*934_*951del
ENST00000688308.1:c.823_840del	ENSP00000508752.1:p.Val275_Ile280del
ENST00000688922.1:c.744_761del
ENST00000693560.1:c.1342_1359del	ENSP00000509861.1:p.Val448_Ile453del
ENST00000371953.8:c.823_840del MANE Select	ENSP00000361021.3:p.Val275_Ile280del
ENST00000371953.7:c.823_840del	ENSP00000361021.3:p.Val275_Ile280del
ENST00000472832.2:c.250_267del	ENSP00000483066.1:p.Val84_Ile89del
NM_000314.5:c.823_840del	NP_000305.3:p.Val275_Ile280del
NM_000314.6:c.823_840del	NP_000305.3:p.Val275_Ile280del
NM_001304717.2:c.1342_1359del	NP_001291646.2:p.Val448_Ile453del
NM_001304718.1:c.232_249del	NP_001291647.1:p.Val78_Ile83del
XM_006717926.2:c.778_795del	XP_006717989.1:p.Val260_Ile265del
XM_011539981.1:c.823_840del	XP_011538283.1:p.Val275_Ile280del
XM_011539982.1:c.727_744del	XP_011538284.1:p.Val243_Ile248del
XR_945791.1:n.1393_1410del
NM_000314.7:c.823_840del	NP_000305.3:p.Val275_Ile280del
NM_001304717.5:c.1342_1359del	NP_001291646.4:p.Val448_Ile453del
NM_001304718.2:c.232_249del	NP_001291647.1:p.Val78_Ile83del
NM_000314.8:c.823_840del MANE Select	NP_000305.3:p.Val275_Ile280del