Canonical Allele Identifier: CA2579926571

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87961114_87961115delinsGG , CM000672.2:g.87961114_87961115delinsGG	GRCh38
NC_000010.10:g.89720871_89720872delinsGG , CM000672.1:g.89720871_89720872delinsGG	GRCh37
NC_000010.9:g.89710851_89710852delinsGG	NCBI36
NG_007466.2:g.102676_102677delinsGG , LRG_311:g.102676_102677delinsGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.1115_1116delinsGG	ENSP00000514759.2:p.Phe372Trp
ENST00000710265.1:c.1022_1023delinsGG	ENSP00000518161.1:p.Phe341Trp
ENST00000472832.3:c.1022_1023delinsGG	ENSP00000483066.2:p.Phe341Trp
ENST00000688158.2:n.1757_1758delinsGG
ENST00000688922.2:c.*852_*853delinsGG	ENSP00000508742.2:n.*852_*853delinsGG
ENST00000700021.1:c.977_978delinsGG	ENSP00000514757.1:p.Phe326Trp
ENST00000700022.1:c.*361_*362delinsGG	ENSP00000514758.1:n.*361_*362delinsGG
ENST00000700023.1:n.2180_2181delinsGG
ENST00000700024.1:n.2414_2415delinsGG
ENST00000700025.1:n.1791_1792delinsGG
ENST00000700026.1:n.659_660delinsGG
ENST00000706954.1:c.1022_1023delinsGG	ENSP00000516674.1:p.Phe341Trp
ENST00000706955.1:c.*1057_*1058delinsGG	ENSP00000516675.1:n.*1057_*1058delinsGG
ENST00000686459.1:c.*608_*609delinsGG	ENSP00000508909.1:n.*608_*609delinsGG
ENST00000688158.1:c.*1133_*1134delinsGG	ENSP00000509254.1:n.*1133_*1134delinsGG
ENST00000688308.1:c.1022_1023delinsGG	ENSP00000508752.1:p.Phe341Trp
ENST00000688922.1:c.943_944delinsGG
ENST00000693560.1:c.1541_1542delinsGG	ENSP00000509861.1:p.Phe514Trp
ENST00000371953.8:c.1022_1023delinsGG MANE Select	ENSP00000361021.3:p.Phe341Trp
ENST00000371953.7:c.1022_1023delinsGG	ENSP00000361021.3:p.Phe341Trp
ENST00000472832.2:c.449_450delinsGG	ENSP00000483066.1:p.Phe150Trp
NM_000314.5:c.1022_1023delinsGG	NP_000305.3:p.Phe341Trp
NM_000314.6:c.1022_1023delinsGG	NP_000305.3:p.Phe341Trp
NM_001304717.2:c.1541_1542delinsGG	NP_001291646.2:p.Phe514Trp
NM_001304718.1:c.431_432delinsGG	NP_001291647.1:p.Phe144Trp
XM_006717926.2:c.977_978delinsGG	XP_006717989.1:p.Phe326Trp
XM_011539981.1:c.1022_1023delinsGG	XP_011538283.1:p.Phe341Trp
XM_011539982.1:c.926_927delinsGG	XP_011538284.1:p.Phe309Trp
XR_945791.1:n.1592_1593delinsGG
NM_000314.7:c.1022_1023delinsGG	NP_000305.3:p.Phe341Trp
NM_001304717.5:c.1541_1542delinsGG	NP_001291646.4:p.Phe514Trp
NM_001304718.2:c.431_432delinsGG	NP_001291647.1:p.Phe144Trp
NM_000314.8:c.1022_1023delinsGG MANE Select	NP_000305.3:p.Phe341Trp