Canonical Allele Identifier: CA891839841

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87957957_87957959delinsATT , CM000672.2:g.87957957_87957959delinsATT	GRCh38
NC_000010.10:g.89717714_89717716delinsATT , CM000672.1:g.89717714_89717716delinsATT	GRCh37
NC_000010.9:g.89707694_89707696delinsATT	NCBI36
NG_007466.2:g.99519_99521delinsATT , LRG_311:g.99519_99521delinsATT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.739_741delinsATT	ENSP00000514759.2:p.Leu247Ile
ENST00000710265.1:c.739_741delinsATT	ENSP00000518161.1:p.Leu247Ile
ENST00000472832.3:c.739_741delinsATT	ENSP00000483066.2:p.Leu247Ile
ENST00000688158.2:n.1474_1476delinsATT
ENST00000688922.2:c.*569_*571delinsATT	ENSP00000508742.2:n.*569_*571delinsATT
ENST00000700021.1:c.694_696delinsATT	ENSP00000514757.1:p.Leu232Ile
ENST00000700022.1:c.*78_*80delinsATT	ENSP00000514758.1:n.*78_*80delinsATT
ENST00000700023.1:n.1897_1899delinsATT
ENST00000700024.1:n.2131_2133delinsATT
ENST00000700025.1:n.1508_1510delinsATT
ENST00000700026.1:n.376_378delinsATT
ENST00000700029.1:c.573_575delinsATT
ENST00000706954.1:c.739_741delinsATT	ENSP00000516674.1:p.Leu247Ile
ENST00000706955.1:c.*774_*776delinsATT	ENSP00000516675.1:n.*774_*776delinsATT
ENST00000686459.1:c.*325_*327delinsATT	ENSP00000508909.1:n.*325_*327delinsATT
ENST00000688158.1:c.*850_*852delinsATT	ENSP00000509254.1:n.*850_*852delinsATT
ENST00000688308.1:c.739_741delinsATT	ENSP00000508752.1:p.Leu247Ile
ENST00000688922.1:c.660_662delinsATT
ENST00000693560.1:c.1258_1260delinsATT	ENSP00000509861.1:p.Leu420Ile
ENST00000371953.8:c.739_741delinsATT MANE Select	ENSP00000361021.3:p.Leu247Ile
ENST00000371953.7:c.739_741delinsATT	ENSP00000361021.3:p.Leu247Ile
ENST00000472832.2:c.166_168delinsATT	ENSP00000483066.1:p.Leu56Ile
NM_000314.5:c.739_741delinsATT	NP_000305.3:p.Leu247Ile
NM_000314.6:c.739_741delinsATT	NP_000305.3:p.Leu247Ile
NM_001304717.2:c.1258_1260delinsATT	NP_001291646.2:p.Leu420Ile
NM_001304718.1:c.148_150delinsATT	NP_001291647.1:p.Leu50Ile
XM_006717926.2:c.694_696delinsATT	XP_006717989.1:p.Leu232Ile
XM_011539981.1:c.739_741delinsATT	XP_011538283.1:p.Leu247Ile
XM_011539982.1:c.643_645delinsATT	XP_011538284.1:p.Leu215Ile
XR_945791.1:n.1309_1311delinsATT
NM_000314.7:c.739_741delinsATT	NP_000305.3:p.Leu247Ile
NM_001304717.5:c.1258_1260delinsATT	NP_001291646.4:p.Leu420Ile
NM_001304718.2:c.148_150delinsATT	NP_001291647.1:p.Leu50Ile
NM_000314.8:c.739_741delinsATT MANE Select	NP_000305.3:p.Leu247Ile