Canonical Allele Identifier: CA891841445

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87961113_87961115delinsGAA , CM000672.2:g.87961113_87961115delinsGAA	GRCh38
NC_000010.10:g.89720870_89720872delinsGAA , CM000672.1:g.89720870_89720872delinsGAA	GRCh37
NC_000010.9:g.89710850_89710852delinsGAA	NCBI36
NG_007466.2:g.102675_102677delinsGAA , LRG_311:g.102675_102677delinsGAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.1114_1116delinsGAA	ENSP00000514759.2:p.Phe372Glu
ENST00000710265.1:c.1021_1023delinsGAA	ENSP00000518161.1:p.Phe341Glu
ENST00000472832.3:c.1021_1023delinsGAA	ENSP00000483066.2:p.Phe341Glu
ENST00000688158.2:n.1756_1758delinsGAA
ENST00000688922.2:c.*851_*853delinsGAA	ENSP00000508742.2:n.*851_*853delinsGAA
ENST00000700021.1:c.976_978delinsGAA	ENSP00000514757.1:p.Phe326Glu
ENST00000700022.1:c.*360_*362delinsGAA	ENSP00000514758.1:n.*360_*362delinsGAA
ENST00000700023.1:n.2179_2181delinsGAA
ENST00000700024.1:n.2413_2415delinsGAA
ENST00000700025.1:n.1790_1792delinsGAA
ENST00000700026.1:n.658_660delinsGAA
ENST00000706954.1:c.1021_1023delinsGAA	ENSP00000516674.1:p.Phe341Glu
ENST00000706955.1:c.*1056_*1058delinsGAA	ENSP00000516675.1:n.*1056_*1058delinsGAA
ENST00000686459.1:c.*607_*609delinsGAA	ENSP00000508909.1:n.*607_*609delinsGAA
ENST00000688158.1:c.*1132_*1134delinsGAA	ENSP00000509254.1:n.*1132_*1134delinsGAA
ENST00000688308.1:c.1021_1023delinsGAA	ENSP00000508752.1:p.Phe341Glu
ENST00000688922.1:c.942_944delinsGAA
ENST00000693560.1:c.1540_1542delinsGAA	ENSP00000509861.1:p.Phe514Glu
ENST00000371953.8:c.1021_1023delinsGAA MANE Select	ENSP00000361021.3:p.Phe341Glu
ENST00000371953.7:c.1021_1023delinsGAA	ENSP00000361021.3:p.Phe341Glu
ENST00000472832.2:c.448_450delinsGAA	ENSP00000483066.1:p.Phe150Glu
NM_000314.5:c.1021_1023delinsGAA	NP_000305.3:p.Phe341Glu
NM_000314.6:c.1021_1023delinsGAA	NP_000305.3:p.Phe341Glu
NM_001304717.2:c.1540_1542delinsGAA	NP_001291646.2:p.Phe514Glu
NM_001304718.1:c.430_432delinsGAA	NP_001291647.1:p.Phe144Glu
XM_006717926.2:c.976_978delinsGAA	XP_006717989.1:p.Phe326Glu
XM_011539981.1:c.1021_1023delinsGAA	XP_011538283.1:p.Phe341Glu
XM_011539982.1:c.925_927delinsGAA	XP_011538284.1:p.Phe309Glu
XR_945791.1:n.1591_1593delinsGAA
NM_000314.7:c.1021_1023delinsGAA	NP_000305.3:p.Phe341Glu
NM_001304717.5:c.1540_1542delinsGAA	NP_001291646.4:p.Phe514Glu
NM_001304718.2:c.430_432delinsGAA	NP_001291647.1:p.Phe144Glu
NM_000314.8:c.1021_1023delinsGAA MANE Select	NP_000305.3:p.Phe341Glu