Canonical Allele Identifier: CA891838183

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87965449_87965450delinsTT , CM000672.2:g.87965449_87965450delinsTT	GRCh38
NC_000010.10:g.89725206_89725207delinsTT , CM000672.1:g.89725206_89725207delinsTT	GRCh37
NC_000010.9:g.89715186_89715187delinsTT	NCBI36
NG_007466.2:g.107011_107012delinsTT , LRG_311:g.107011_107012delinsTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.1282_1283delinsTT	ENSP00000514759.2:p.His428Phe
ENST00000710265.1:c.*218_*219delinsTT	ENSP00000518161.1:n.*218_*219delinsTT
ENST00000688158.2:n.1924_1925delinsTT
ENST00000688922.2:c.*1019_*1020delinsTT	ENSP00000508742.2:n.*1019_*1020delinsTT
ENST00000700021.1:c.1144_1145delinsTT	ENSP00000514757.1:p.His382Phe
ENST00000700022.1:c.*528_*529delinsTT	ENSP00000514758.1:n.*528_*529delinsTT
ENST00000700023.1:n.2347_2348delinsTT
ENST00000700024.1:n.2581_2582delinsTT
ENST00000706954.1:c.1189_1190delinsTT	ENSP00000516674.1:p.His397Phe
ENST00000706955.1:c.*1224_*1225delinsTT	ENSP00000516675.1:n.*1224_*1225delinsTT
ENST00000686459.1:c.*775_*776delinsTT	ENSP00000508909.1:n.*775_*776delinsTT
ENST00000688158.1:c.*1300_*1301delinsTT	ENSP00000509254.1:n.*1300_*1301delinsTT
ENST00000688308.1:c.1189_1190delinsTT	ENSP00000508752.1:p.His397Phe
ENST00000688922.1:c.1110_1111delinsTT
ENST00000693560.1:c.1708_1709delinsTT	ENSP00000509861.1:p.His570Phe
ENST00000371953.8:c.1189_1190delinsTT MANE Select	ENSP00000361021.3:p.His397Phe
ENST00000371953.7:c.1189_1190delinsTT	ENSP00000361021.3:p.His397Phe
NM_000314.5:c.1189_1190delinsTT	NP_000305.3:p.His397Phe
NM_000314.6:c.1189_1190delinsTT	NP_000305.3:p.His397Phe
NM_001304717.2:c.1708_1709delinsTT	NP_001291646.2:p.His570Phe
NM_001304718.1:c.598_599delinsTT	NP_001291647.1:p.His200Phe
XM_006717926.2:c.1144_1145delinsTT	XP_006717989.1:p.His382Phe
XM_011539982.1:c.1093_1094delinsTT	XP_011538284.1:p.His365Phe
XR_945791.1:n.1759_1760delinsTT
NM_000314.7:c.1189_1190delinsTT	NP_000305.3:p.His397Phe
NM_001304717.5:c.1708_1709delinsTT	NP_001291646.4:p.His570Phe
NM_001304718.2:c.598_599delinsTT	NP_001291647.1:p.His200Phe
NM_000314.8:c.1189_1190delinsTT MANE Select	NP_000305.3:p.His397Phe