Canonical Allele Identifier: CA891839839

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87957957_87957959delinsAAT , CM000672.2:g.87957957_87957959delinsAAT	GRCh38
NC_000010.10:g.89717714_89717716delinsAAT , CM000672.1:g.89717714_89717716delinsAAT	GRCh37
NC_000010.9:g.89707694_89707696delinsAAT	NCBI36
NG_007466.2:g.99519_99521delinsAAT , LRG_311:g.99519_99521delinsAAT

Transcript Alleles

HGVS	Amino-acid change
ENST00000700029.2:c.739_741delinsAAT	ENSP00000514759.2:p.Leu247Asn
ENST00000710265.1:c.739_741delinsAAT	ENSP00000518161.1:p.Leu247Asn
ENST00000472832.3:c.739_741delinsAAT	ENSP00000483066.2:p.Leu247Asn
ENST00000688158.2:n.1474_1476delinsAAT
ENST00000688922.2:c.*569_*571delinsAAT	ENSP00000508742.2:n.*569_*571delinsAAT
ENST00000700021.1:c.694_696delinsAAT	ENSP00000514757.1:p.Leu232Asn
ENST00000700022.1:c.*78_*80delinsAAT	ENSP00000514758.1:n.*78_*80delinsAAT
ENST00000700023.1:n.1897_1899delinsAAT
ENST00000700024.1:n.2131_2133delinsAAT
ENST00000700025.1:n.1508_1510delinsAAT
ENST00000700026.1:n.376_378delinsAAT
ENST00000700029.1:c.573_575delinsAAT
ENST00000706954.1:c.739_741delinsAAT	ENSP00000516674.1:p.Leu247Asn
ENST00000706955.1:c.*774_*776delinsAAT	ENSP00000516675.1:n.*774_*776delinsAAT
ENST00000686459.1:c.*325_*327delinsAAT	ENSP00000508909.1:n.*325_*327delinsAAT
ENST00000688158.1:c.*850_*852delinsAAT	ENSP00000509254.1:n.*850_*852delinsAAT
ENST00000688308.1:c.739_741delinsAAT	ENSP00000508752.1:p.Leu247Asn
ENST00000688922.1:c.660_662delinsAAT
ENST00000693560.1:c.1258_1260delinsAAT	ENSP00000509861.1:p.Leu420Asn
ENST00000371953.8:c.739_741delinsAAT MANE Select	ENSP00000361021.3:p.Leu247Asn
ENST00000371953.7:c.739_741delinsAAT	ENSP00000361021.3:p.Leu247Asn
ENST00000472832.2:c.166_168delinsAAT	ENSP00000483066.1:p.Leu56Asn
NM_000314.5:c.739_741delinsAAT	NP_000305.3:p.Leu247Asn
NM_000314.6:c.739_741delinsAAT	NP_000305.3:p.Leu247Asn
NM_001304717.2:c.1258_1260delinsAAT	NP_001291646.2:p.Leu420Asn
NM_001304718.1:c.148_150delinsAAT	NP_001291647.1:p.Leu50Asn
XM_006717926.2:c.694_696delinsAAT	XP_006717989.1:p.Leu232Asn
XM_011539981.1:c.739_741delinsAAT	XP_011538283.1:p.Leu247Asn
XM_011539982.1:c.643_645delinsAAT	XP_011538284.1:p.Leu215Asn
XR_945791.1:n.1309_1311delinsAAT
NM_000314.7:c.739_741delinsAAT	NP_000305.3:p.Leu247Asn
NM_001304717.5:c.1258_1260delinsAAT	NP_001291646.4:p.Leu420Asn
NM_001304718.2:c.148_150delinsAAT	NP_001291647.1:p.Leu50Asn
NM_000314.8:c.739_741delinsAAT MANE Select	NP_000305.3:p.Leu247Asn