Canonical Allele Identifier: CA891836380

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87961032_87961034delinsTTT , CM000672.2:g.87961032_87961034delinsTTT	GRCh38
NC_000010.10:g.89720789_89720791delinsTTT , CM000672.1:g.89720789_89720791delinsTTT	GRCh37
NC_000010.9:g.89710769_89710771delinsTTT	NCBI36
NG_007466.2:g.102594_102596delinsTTT , LRG_311:g.102594_102596delinsTTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.1033_1035delinsTTT	ENSP00000514759.2:p.Glu345Phe
ENST00000710265.1:c.940_942delinsTTT	ENSP00000518161.1:p.Glu314Phe
ENST00000472832.3:c.940_942delinsTTT	ENSP00000483066.2:p.Glu314Phe
ENST00000688158.2:n.1675_1677delinsTTT
ENST00000688922.2:c.*770_*772delinsTTT	ENSP00000508742.2:n.*770_*772delinsTTT
ENST00000700021.1:c.895_897delinsTTT	ENSP00000514757.1:p.Glu299Phe
ENST00000700022.1:c.*279_*281delinsTTT	ENSP00000514758.1:n.*279_*281delinsTTT
ENST00000700023.1:n.2098_2100delinsTTT
ENST00000700024.1:n.2332_2334delinsTTT
ENST00000700025.1:n.1709_1711delinsTTT
ENST00000700026.1:n.577_579delinsTTT
ENST00000706954.1:c.940_942delinsTTT	ENSP00000516674.1:p.Glu314Phe
ENST00000706955.1:c.*975_*977delinsTTT	ENSP00000516675.1:n.*975_*977delinsTTT
ENST00000686459.1:c.*526_*528delinsTTT	ENSP00000508909.1:n.*526_*528delinsTTT
ENST00000688158.1:c.*1051_*1053delinsTTT	ENSP00000509254.1:n.*1051_*1053delinsTTT
ENST00000688308.1:c.940_942delinsTTT	ENSP00000508752.1:p.Glu314Phe
ENST00000688922.1:c.861_863delinsTTT
ENST00000693560.1:c.1459_1461delinsTTT	ENSP00000509861.1:p.Glu487Phe
ENST00000371953.8:c.940_942delinsTTT MANE Select	ENSP00000361021.3:p.Glu314Phe
ENST00000371953.7:c.940_942delinsTTT	ENSP00000361021.3:p.Glu314Phe
ENST00000472832.2:c.367_369delinsTTT	ENSP00000483066.1:p.Glu123Phe
NM_000314.5:c.940_942delinsTTT	NP_000305.3:p.Glu314Phe
NM_000314.6:c.940_942delinsTTT	NP_000305.3:p.Glu314Phe
NM_001304717.2:c.1459_1461delinsTTT	NP_001291646.2:p.Glu487Phe
NM_001304718.1:c.349_351delinsTTT	NP_001291647.1:p.Glu117Phe
XM_006717926.2:c.895_897delinsTTT	XP_006717989.1:p.Glu299Phe
XM_011539981.1:c.940_942delinsTTT	XP_011538283.1:p.Glu314Phe
XM_011539982.1:c.844_846delinsTTT	XP_011538284.1:p.Glu282Phe
XR_945791.1:n.1510_1512delinsTTT
NM_000314.7:c.940_942delinsTTT	NP_000305.3:p.Glu314Phe
NM_001304717.5:c.1459_1461delinsTTT	NP_001291646.4:p.Glu487Phe
NM_001304718.2:c.349_351delinsTTT	NP_001291647.1:p.Glu117Phe
NM_000314.8:c.940_942delinsTTT MANE Select	NP_000305.3:p.Glu314Phe