Canonical Allele Identifier: CA2579926410

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87965401_87965403delinsTTT , CM000672.2:g.87965401_87965403delinsTTT	GRCh38
NC_000010.10:g.89725158_89725160delinsTTT , CM000672.1:g.89725158_89725160delinsTTT	GRCh37
NC_000010.9:g.89715138_89715140delinsTTT	NCBI36
NG_007466.2:g.106963_106965delinsTTT , LRG_311:g.106963_106965delinsTTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.1234_1236delinsTTT	ENSP00000514759.2:p.Asp412Phe
ENST00000710265.1:c.*170_*172delinsTTT	ENSP00000518161.1:n.*170_*172delinsTTT
ENST00000688158.2:n.1876_1878delinsTTT
ENST00000688922.2:c.*971_*973delinsTTT	ENSP00000508742.2:n.*971_*973delinsTTT
ENST00000700021.1:c.1096_1098delinsTTT	ENSP00000514757.1:p.Asp366Phe
ENST00000700022.1:c.*480_*482delinsTTT	ENSP00000514758.1:n.*480_*482delinsTTT
ENST00000700023.1:n.2299_2301delinsTTT
ENST00000700024.1:n.2533_2535delinsTTT
ENST00000706954.1:c.1141_1143delinsTTT	ENSP00000516674.1:p.Asp381Phe
ENST00000706955.1:c.*1176_*1178delinsTTT	ENSP00000516675.1:n.*1176_*1178delinsTTT
ENST00000686459.1:c.*727_*729delinsTTT	ENSP00000508909.1:n.*727_*729delinsTTT
ENST00000688158.1:c.*1252_*1254delinsTTT	ENSP00000509254.1:n.*1252_*1254delinsTTT
ENST00000688308.1:c.1141_1143delinsTTT	ENSP00000508752.1:p.Asp381Phe
ENST00000688922.1:c.1062_1064delinsTTT
ENST00000693560.1:c.1660_1662delinsTTT	ENSP00000509861.1:p.Asp554Phe
ENST00000371953.8:c.1141_1143delinsTTT MANE Select	ENSP00000361021.3:p.Asp381Phe
ENST00000371953.7:c.1141_1143delinsTTT	ENSP00000361021.3:p.Asp381Phe
NM_000314.5:c.1141_1143delinsTTT	NP_000305.3:p.Asp381Phe
NM_000314.6:c.1141_1143delinsTTT	NP_000305.3:p.Asp381Phe
NM_001304717.2:c.1660_1662delinsTTT	NP_001291646.2:p.Asp554Phe
NM_001304718.1:c.550_552delinsTTT	NP_001291647.1:p.Asp184Phe
XM_006717926.2:c.1096_1098delinsTTT	XP_006717989.1:p.Asp366Phe
XM_011539982.1:c.1045_1047delinsTTT	XP_011538284.1:p.Asp349Phe
XR_945791.1:n.1711_1713delinsTTT
NM_000314.7:c.1141_1143delinsTTT	NP_000305.3:p.Asp381Phe
NM_001304717.5:c.1660_1662delinsTTT	NP_001291646.4:p.Asp554Phe
NM_001304718.2:c.550_552delinsTTT	NP_001291647.1:p.Asp184Phe
NM_000314.8:c.1141_1143delinsTTT MANE Select	NP_000305.3:p.Asp381Phe