Canonical Allele Identifier: CA891834741

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87960930_87960932delinsGCT , CM000672.2:g.87960930_87960932delinsGCT	GRCh38
NC_000010.10:g.89720687_89720689delinsGCT , CM000672.1:g.89720687_89720689delinsGCT	GRCh37
NC_000010.9:g.89710667_89710669delinsGCT	NCBI36
NG_007466.2:g.102492_102494delinsGCT , LRG_311:g.102492_102494delinsGCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.931_933delinsGCT	ENSP00000514759.2:p.Ile311Ala
ENST00000710265.1:c.838_840delinsGCT	ENSP00000518161.1:p.Ile280Ala
ENST00000472832.3:c.838_840delinsGCT	ENSP00000483066.2:p.Ile280Ala
ENST00000688158.2:n.1573_1575delinsGCT
ENST00000688922.2:c.*668_*670delinsGCT	ENSP00000508742.2:n.*668_*670delinsGCT
ENST00000700021.1:c.793_795delinsGCT	ENSP00000514757.1:p.Ile265Ala
ENST00000700022.1:c.*177_*179delinsGCT	ENSP00000514758.1:n.*177_*179delinsGCT
ENST00000700023.1:n.1996_1998delinsGCT
ENST00000700024.1:n.2230_2232delinsGCT
ENST00000700025.1:n.1607_1609delinsGCT
ENST00000700026.1:n.475_477delinsGCT
ENST00000700029.1:c.765_767delinsGCT
ENST00000706954.1:c.838_840delinsGCT	ENSP00000516674.1:p.Ile280Ala
ENST00000706955.1:c.*873_*875delinsGCT	ENSP00000516675.1:n.*873_*875delinsGCT
ENST00000686459.1:c.*424_*426delinsGCT	ENSP00000508909.1:n.*424_*426delinsGCT
ENST00000688158.1:c.*949_*951delinsGCT	ENSP00000509254.1:n.*949_*951delinsGCT
ENST00000688308.1:c.838_840delinsGCT	ENSP00000508752.1:p.Ile280Ala
ENST00000688922.1:c.759_761delinsGCT
ENST00000693560.1:c.1357_1359delinsGCT	ENSP00000509861.1:p.Ile453Ala
ENST00000371953.8:c.838_840delinsGCT MANE Select	ENSP00000361021.3:p.Ile280Ala
ENST00000371953.7:c.838_840delinsGCT	ENSP00000361021.3:p.Ile280Ala
ENST00000472832.2:c.265_267delinsGCT	ENSP00000483066.1:p.Ile89Ala
NM_000314.5:c.838_840delinsGCT	NP_000305.3:p.Ile280Ala
NM_000314.6:c.838_840delinsGCT	NP_000305.3:p.Ile280Ala
NM_001304717.2:c.1357_1359delinsGCT	NP_001291646.2:p.Ile453Ala
NM_001304718.1:c.247_249delinsGCT	NP_001291647.1:p.Ile83Ala
XM_006717926.2:c.793_795delinsGCT	XP_006717989.1:p.Ile265Ala
XM_011539981.1:c.838_840delinsGCT	XP_011538283.1:p.Ile280Ala
XM_011539982.1:c.742_744delinsGCT	XP_011538284.1:p.Ile248Ala
XR_945791.1:n.1408_1410delinsGCT
NM_000314.7:c.838_840delinsGCT	NP_000305.3:p.Ile280Ala
NM_001304717.5:c.1357_1359delinsGCT	NP_001291646.4:p.Ile453Ala
NM_001304718.2:c.247_249delinsGCT	NP_001291647.1:p.Ile83Ala
NM_000314.8:c.838_840delinsGCT MANE Select	NP_000305.3:p.Ile280Ala