Canonical Allele Identifier: CA891841717

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87965458_87965459delinsGC , CM000672.2:g.87965458_87965459delinsGC	GRCh38
NC_000010.10:g.89725215_89725216delinsGC , CM000672.1:g.89725215_89725216delinsGC	GRCh37
NC_000010.9:g.89715195_89715196delinsGC	NCBI36
NG_007466.2:g.107020_107021delinsGC , LRG_311:g.107020_107021delinsGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.1291_1292delinsGC	ENSP00000514759.2:p.Ile431Ala
ENST00000710265.1:c.*227_*228delinsGC	ENSP00000518161.1:n.*227_*228delinsGC
ENST00000688158.2:n.1933_1934delinsGC
ENST00000688922.2:c.*1028_*1029delinsGC	ENSP00000508742.2:n.*1028_*1029delinsGC
ENST00000700021.1:c.1153_1154delinsGC	ENSP00000514757.1:p.Ile385Ala
ENST00000700022.1:c.*537_*538delinsGC	ENSP00000514758.1:n.*537_*538delinsGC
ENST00000700023.1:n.2356_2357delinsGC
ENST00000700024.1:n.2590_2591delinsGC
ENST00000706954.1:c.1198_1199delinsGC	ENSP00000516674.1:p.Ile400Ala
ENST00000706955.1:c.*1233_*1234delinsGC	ENSP00000516675.1:n.*1233_*1234delinsGC
ENST00000686459.1:c.*784_*785delinsGC	ENSP00000508909.1:n.*784_*785delinsGC
ENST00000688158.1:c.*1309_*1310delinsGC	ENSP00000509254.1:n.*1309_*1310delinsGC
ENST00000688308.1:c.1198_1199delinsGC	ENSP00000508752.1:p.Ile400Ala
ENST00000688922.1:c.1119_1120delinsGC
ENST00000693560.1:c.1717_1718delinsGC	ENSP00000509861.1:p.Ile573Ala
ENST00000371953.8:c.1198_1199delinsGC MANE Select	ENSP00000361021.3:p.Ile400Ala
ENST00000371953.7:c.1198_1199delinsGC	ENSP00000361021.3:p.Ile400Ala
NM_000314.5:c.1198_1199delinsGC	NP_000305.3:p.Ile400Ala
NM_000314.6:c.1198_1199delinsGC	NP_000305.3:p.Ile400Ala
NM_001304717.2:c.1717_1718delinsGC	NP_001291646.2:p.Ile573Ala
NM_001304718.1:c.607_608delinsGC	NP_001291647.1:p.Ile203Ala
XM_006717926.2:c.1153_1154delinsGC	XP_006717989.1:p.Ile385Ala
XM_011539982.1:c.1102_1103delinsGC	XP_011538284.1:p.Ile368Ala
XR_945791.1:n.1768_1769delinsGC
NM_000314.7:c.1198_1199delinsGC	NP_000305.3:p.Ile400Ala
NM_001304717.5:c.1717_1718delinsGC	NP_001291646.4:p.Ile573Ala
NM_001304718.2:c.607_608delinsGC	NP_001291647.1:p.Ile203Ala
NM_000314.8:c.1198_1199delinsGC MANE Select	NP_000305.3:p.Ile400Ala