Canonical Allele Identifier: CA891837260

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87965332_87965334delinsAAT , CM000672.2:g.87965332_87965334delinsAAT	GRCh38
NC_000010.10:g.89725089_89725091delinsAAT , CM000672.1:g.89725089_89725091delinsAAT	GRCh37
NC_000010.9:g.89715069_89715071delinsAAT	NCBI36
NG_007466.2:g.106894_106896delinsAAT , LRG_311:g.106894_106896delinsAAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.1165_1167delinsAAT	ENSP00000514759.2:p.Glu389Asn
ENST00000710265.1:c.*101_*103delinsAAT	ENSP00000518161.1:n.*101_*103delinsAAT
ENST00000688158.2:n.1807_1809delinsAAT
ENST00000688922.2:c.*902_*904delinsAAT	ENSP00000508742.2:n.*902_*904delinsAAT
ENST00000700021.1:c.1027_1029delinsAAT	ENSP00000514757.1:p.Glu343Asn
ENST00000700022.1:c.*411_*413delinsAAT	ENSP00000514758.1:n.*411_*413delinsAAT
ENST00000700023.1:n.2230_2232delinsAAT
ENST00000700024.1:n.2464_2466delinsAAT
ENST00000706954.1:c.1072_1074delinsAAT	ENSP00000516674.1:p.Glu358Asn
ENST00000706955.1:c.*1107_*1109delinsAAT	ENSP00000516675.1:n.*1107_*1109delinsAAT
ENST00000686459.1:c.*658_*660delinsAAT	ENSP00000508909.1:n.*658_*660delinsAAT
ENST00000688158.1:c.*1183_*1185delinsAAT	ENSP00000509254.1:n.*1183_*1185delinsAAT
ENST00000688308.1:c.1072_1074delinsAAT	ENSP00000508752.1:p.Glu358Asn
ENST00000688922.1:c.993_995delinsAAT
ENST00000693560.1:c.1591_1593delinsAAT	ENSP00000509861.1:p.Glu531Asn
ENST00000371953.8:c.1072_1074delinsAAT MANE Select	ENSP00000361021.3:p.Glu358Asn
ENST00000371953.7:c.1072_1074delinsAAT	ENSP00000361021.3:p.Glu358Asn
NM_000314.5:c.1072_1074delinsAAT	NP_000305.3:p.Glu358Asn
NM_000314.6:c.1072_1074delinsAAT	NP_000305.3:p.Glu358Asn
NM_001304717.2:c.1591_1593delinsAAT	NP_001291646.2:p.Glu531Asn
NM_001304718.1:c.481_483delinsAAT	NP_001291647.1:p.Glu161Asn
XM_006717926.2:c.1027_1029delinsAAT	XP_006717989.1:p.Glu343Asn
XM_011539982.1:c.976_978delinsAAT	XP_011538284.1:p.Glu326Asn
XR_945791.1:n.1642_1644delinsAAT
NM_000314.7:c.1072_1074delinsAAT	NP_000305.3:p.Glu358Asn
NM_001304717.5:c.1591_1593delinsAAT	NP_001291646.4:p.Glu531Asn
NM_001304718.2:c.481_483delinsAAT	NP_001291647.1:p.Glu161Asn
NM_000314.8:c.1072_1074delinsAAT MANE Select	NP_000305.3:p.Glu358Asn