Canonical Allele Identifier: CA1926190050

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87961021_87961022delinsAT , CM000672.2:g.87961021_87961022delinsAT	GRCh38
NC_000010.10:g.89720778_89720779delinsAT , CM000672.1:g.89720778_89720779delinsAT	GRCh37
NC_000010.9:g.89710758_89710759delinsAT	NCBI36
NG_007466.2:g.102583_102584delinsAT , LRG_311:g.102583_102584delinsAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.1022_1023delinsAT	ENSP00000514759.2:p.Asp341=
ENST00000710265.1:c.929_930delinsAT	ENSP00000518161.1:p.Asp310=
ENST00000472832.3:c.929_930delinsAT	ENSP00000483066.2:p.Asp310=
ENST00000688158.2:n.1664_1665delinsAT
ENST00000688922.2:c.*759_*760delinsAT	ENSP00000508742.2:n.*759_*760delinsAT
ENST00000700021.1:c.884_885delinsAT	ENSP00000514757.1:p.Asp295=
ENST00000700022.1:c.*268_*269delinsAT	ENSP00000514758.1:n.*268_*269delinsAT
ENST00000700023.1:n.2087_2088delinsAT
ENST00000700024.1:n.2321_2322delinsAT
ENST00000700025.1:n.1698_1699delinsAT
ENST00000700026.1:n.566_567delinsAT
ENST00000706954.1:c.929_930delinsAT	ENSP00000516674.1:p.Asp310=
ENST00000706955.1:c.*964_*965delinsAT	ENSP00000516675.1:n.*964_*965delinsAT
ENST00000686459.1:c.*515_*516delinsAT	ENSP00000508909.1:n.*515_*516delinsAT
ENST00000688158.1:c.*1040_*1041delinsAT	ENSP00000509254.1:n.*1040_*1041delinsAT
ENST00000688308.1:c.929_930delinsAT	ENSP00000508752.1:p.Asp310=
ENST00000688922.1:c.850_851delinsAT
ENST00000693560.1:c.1448_1449delinsAT	ENSP00000509861.1:p.Asp483=
ENST00000371953.8:c.929_930delinsAT MANE Select	ENSP00000361021.3:p.Asp310=
ENST00000371953.7:c.929_930delinsAT	ENSP00000361021.3:p.Asp310=
ENST00000472832.2:c.356_357delinsAT	ENSP00000483066.1:p.Asp119=
NM_000314.5:c.929_930delinsAT	NP_000305.3:p.Asp310=
NM_000314.6:c.929_930delinsAT	NP_000305.3:p.Asp310=
NM_001304717.2:c.1448_1449delinsAT	NP_001291646.2:p.Asp483=
NM_001304718.1:c.338_339delinsAT	NP_001291647.1:p.Asp113=
XM_006717926.2:c.884_885delinsAT	XP_006717989.1:p.Asp295=
XM_011539981.1:c.929_930delinsAT	XP_011538283.1:p.Asp310=
XM_011539982.1:c.833_834delinsAT	XP_011538284.1:p.Asp278=
XR_945791.1:n.1499_1500delinsAT
NM_000314.7:c.929_930delinsAT	NP_000305.3:p.Asp310=
NM_001304717.5:c.1448_1449delinsAT	NP_001291646.4:p.Asp483=
NM_001304718.2:c.338_339delinsAT	NP_001291647.1:p.Asp113=
NM_000314.8:c.929_930delinsAT MANE Select	NP_000305.3:p.Asp310=