Canonical Allele Identifier: CA891839467

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87957888_87957889delinsCC , CM000672.2:g.87957888_87957889delinsCC	GRCh38
NC_000010.10:g.89717645_89717646delinsCC , CM000672.1:g.89717645_89717646delinsCC	GRCh37
NC_000010.9:g.89707625_89707626delinsCC	NCBI36
NG_007466.2:g.99450_99451delinsCC , LRG_311:g.99450_99451delinsCC

Transcript Alleles

HGVS	Amino-acid change
ENST00000700029.2:c.670_671delinsCC	ENSP00000514759.2:p.Ile224Pro
ENST00000710265.1:c.670_671delinsCC	ENSP00000518161.1:p.Ile224Pro
ENST00000472832.3:c.670_671delinsCC	ENSP00000483066.2:p.Ile224Pro
ENST00000688158.2:n.1405_1406delinsCC
ENST00000688922.2:c.*500_*501delinsCC	ENSP00000508742.2:n.*500_*501delinsCC
ENST00000700021.1:c.625_626delinsCC	ENSP00000514757.1:p.Ile209Pro
ENST00000700022.1:c.*9_*10delinsCC	ENSP00000514758.1:n.*9_*10delinsCC
ENST00000700023.1:n.1828_1829delinsCC
ENST00000700024.1:n.2062_2063delinsCC
ENST00000700025.1:n.1439_1440delinsCC
ENST00000700026.1:n.307_308delinsCC
ENST00000700029.1:c.504_505delinsCC
ENST00000706954.1:c.670_671delinsCC	ENSP00000516674.1:p.Ile224Pro
ENST00000706955.1:c.*705_*706delinsCC	ENSP00000516675.1:n.*705_*706delinsCC
ENST00000686459.1:c.*256_*257delinsCC	ENSP00000508909.1:n.*256_*257delinsCC
ENST00000688158.1:c.*781_*782delinsCC	ENSP00000509254.1:n.*781_*782delinsCC
ENST00000688308.1:c.670_671delinsCC	ENSP00000508752.1:p.Ile224Pro
ENST00000688922.1:c.591_592delinsCC
ENST00000693560.1:c.1189_1190delinsCC	ENSP00000509861.1:p.Ile397Pro
ENST00000371953.8:c.670_671delinsCC MANE Select	ENSP00000361021.3:p.Ile224Pro
ENST00000371953.7:c.670_671delinsCC	ENSP00000361021.3:p.Ile224Pro
ENST00000472832.2:c.97_98delinsCC	ENSP00000483066.1:p.Ile33Pro
NM_000314.5:c.670_671delinsCC	NP_000305.3:p.Ile224Pro
NM_000314.6:c.670_671delinsCC	NP_000305.3:p.Ile224Pro
NM_001304717.2:c.1189_1190delinsCC	NP_001291646.2:p.Ile397Pro
NM_001304718.1:c.79_80delinsCC	NP_001291647.1:p.Ile27Pro
XM_006717926.2:c.625_626delinsCC	XP_006717989.1:p.Ile209Pro
XM_011539981.1:c.670_671delinsCC	XP_011538283.1:p.Ile224Pro
XM_011539982.1:c.574_575delinsCC	XP_011538284.1:p.Ile192Pro
XR_945791.1:n.1240_1241delinsCC
NM_000314.7:c.670_671delinsCC	NP_000305.3:p.Ile224Pro
NM_001304717.5:c.1189_1190delinsCC	NP_001291646.4:p.Ile397Pro
NM_001304718.2:c.79_80delinsCC	NP_001291647.1:p.Ile27Pro
NM_000314.8:c.670_671delinsCC MANE Select	NP_000305.3:p.Ile224Pro