Canonical Allele Identifier: CA891841715

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87965458_87965459delinsGA , CM000672.2:g.87965458_87965459delinsGA	GRCh38
NC_000010.10:g.89725215_89725216delinsGA , CM000672.1:g.89725215_89725216delinsGA	GRCh37
NC_000010.9:g.89715195_89715196delinsGA	NCBI36
NG_007466.2:g.107020_107021delinsGA , LRG_311:g.107020_107021delinsGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.1291_1292delinsGA	ENSP00000514759.2:p.Ile431Asp
ENST00000710265.1:c.*227_*228delinsGA	ENSP00000518161.1:n.*227_*228delinsGA
ENST00000688158.2:n.1933_1934delinsGA
ENST00000688922.2:c.*1028_*1029delinsGA	ENSP00000508742.2:n.*1028_*1029delinsGA
ENST00000700021.1:c.1153_1154delinsGA	ENSP00000514757.1:p.Ile385Asp
ENST00000700022.1:c.*537_*538delinsGA	ENSP00000514758.1:n.*537_*538delinsGA
ENST00000700023.1:n.2356_2357delinsGA
ENST00000700024.1:n.2590_2591delinsGA
ENST00000706954.1:c.1198_1199delinsGA	ENSP00000516674.1:p.Ile400Asp
ENST00000706955.1:c.*1233_*1234delinsGA	ENSP00000516675.1:n.*1233_*1234delinsGA
ENST00000686459.1:c.*784_*785delinsGA	ENSP00000508909.1:n.*784_*785delinsGA
ENST00000688158.1:c.*1309_*1310delinsGA	ENSP00000509254.1:n.*1309_*1310delinsGA
ENST00000688308.1:c.1198_1199delinsGA	ENSP00000508752.1:p.Ile400Asp
ENST00000688922.1:c.1119_1120delinsGA
ENST00000693560.1:c.1717_1718delinsGA	ENSP00000509861.1:p.Ile573Asp
ENST00000371953.8:c.1198_1199delinsGA MANE Select	ENSP00000361021.3:p.Ile400Asp
ENST00000371953.7:c.1198_1199delinsGA	ENSP00000361021.3:p.Ile400Asp
NM_000314.5:c.1198_1199delinsGA	NP_000305.3:p.Ile400Asp
NM_000314.6:c.1198_1199delinsGA	NP_000305.3:p.Ile400Asp
NM_001304717.2:c.1717_1718delinsGA	NP_001291646.2:p.Ile573Asp
NM_001304718.1:c.607_608delinsGA	NP_001291647.1:p.Ile203Asp
XM_006717926.2:c.1153_1154delinsGA	XP_006717989.1:p.Ile385Asp
XM_011539982.1:c.1102_1103delinsGA	XP_011538284.1:p.Ile368Asp
XR_945791.1:n.1768_1769delinsGA
NM_000314.7:c.1198_1199delinsGA	NP_000305.3:p.Ile400Asp
NM_001304717.5:c.1717_1718delinsGA	NP_001291646.4:p.Ile573Asp
NM_001304718.2:c.607_608delinsGA	NP_001291647.1:p.Ile203Asp
NM_000314.8:c.1198_1199delinsGA MANE Select	NP_000305.3:p.Ile400Asp