Canonical Allele Identifier: CA891835337

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87925553_87925554delinsTT , CM000672.2:g.87925553_87925554delinsTT	GRCh38
NC_000010.10:g.89685310_89685311delinsTT , CM000672.1:g.89685310_89685311delinsTT	GRCh37
NC_000010.9:g.89675290_89675291delinsTT	NCBI36
NG_007466.2:g.67115_67116delinsTT , LRG_311:g.67115_67116delinsTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.205_206delinsTT	ENSP00000514759.2:p.Asn69Phe
ENST00000710265.1:c.205_206delinsTT	ENSP00000518161.1:p.Asn69Phe
ENST00000472832.3:c.205_206delinsTT	ENSP00000483066.2:p.Asn69Phe
ENST00000688158.2:n.940_941delinsTT
ENST00000688922.2:c.205_206delinsTT	ENSP00000508742.2:p.Asn69Phe
ENST00000700021.1:c.165-5493_165-5492delinsTT	ENSP00000514757.1:n.165-5493_165-5492delinsTT
ENST00000700022.1:c.205_206delinsTT	ENSP00000514758.1:p.Asn69Phe
ENST00000700029.1:c.39_40delinsTT
ENST00000706954.1:c.205_206delinsTT	ENSP00000516674.1:p.Asn69Phe
ENST00000706955.1:c.*240_*241delinsTT	ENSP00000516675.1:n.*240_*241delinsTT
ENST00000686459.1:c.205_206delinsTT	ENSP00000508909.1:p.Asn69Phe
ENST00000688158.1:c.*316_*317delinsTT	ENSP00000509254.1:n.*316_*317delinsTT
ENST00000688308.1:c.205_206delinsTT	ENSP00000508752.1:p.Asn69Phe
ENST00000688922.1:c.74_75delinsTT
ENST00000693560.1:c.724_725delinsTT	ENSP00000509861.1:p.Asn242Phe
ENST00000371953.8:c.205_206delinsTT MANE Select	ENSP00000361021.3:p.Asn69Phe
ENST00000371953.7:c.205_206delinsTT	ENSP00000361021.3:p.Asn69Phe
ENST00000498703.1:n.31_32delinsTT
ENST00000610634.1:c.103_104delinsTT	ENSP00000477517.1:p.Asn35Phe
NM_000314.5:c.205_206delinsTT	NP_000305.3:p.Asn69Phe
NM_000314.6:c.205_206delinsTT	NP_000305.3:p.Asn69Phe
NM_001304717.2:c.724_725delinsTT	NP_001291646.2:p.Asn242Phe
NM_001304718.1:c.-541-5493_-541-5492delinsTT	NP_001291647.1:n.-541-5493_-541-5492delinsTT
XM_006717926.2:c.165-5493_165-5492delinsTT	XP_006717989.1:n.165-5493_165-5492delinsTT
XM_011539981.1:c.205_206delinsTT	XP_011538283.1:p.Asn69Phe
XM_011539982.1:c.109_110delinsTT	XP_011538284.1:p.Asn37Phe
XR_945789.1:n.917_918delinsTT
XR_945790.1:n.917_918delinsTT
XR_945791.1:n.917_918delinsTT
NM_000314.7:c.205_206delinsTT	NP_000305.3:p.Asn69Phe
NM_001304717.5:c.724_725delinsTT	NP_001291646.4:p.Asn242Phe
NM_001304718.2:c.-541-5493_-541-5492delinsTT	NP_001291647.1:n.-541-5493_-541-5492delinsTT
NM_000314.8:c.205_206delinsTT MANE Select	NP_000305.3:p.Asn69Phe