Canonical Allele Identifier: CA891835936

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87961002_87961004delinsATT , CM000672.2:g.87961002_87961004delinsATT	GRCh38
NC_000010.10:g.89720759_89720761delinsATT , CM000672.1:g.89720759_89720761delinsATT	GRCh37
NC_000010.9:g.89710739_89710741delinsATT	NCBI36
NG_007466.2:g.102564_102566delinsATT , LRG_311:g.102564_102566delinsATT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.1003_1005delinsATT	ENSP00000514759.2:p.Cys335Ile
ENST00000710265.1:c.910_912delinsATT	ENSP00000518161.1:p.Cys304Ile
ENST00000472832.3:c.910_912delinsATT	ENSP00000483066.2:p.Cys304Ile
ENST00000688158.2:n.1645_1647delinsATT
ENST00000688922.2:c.*740_*742delinsATT	ENSP00000508742.2:n.*740_*742delinsATT
ENST00000700021.1:c.865_867delinsATT	ENSP00000514757.1:p.Cys289Ile
ENST00000700022.1:c.*249_*251delinsATT	ENSP00000514758.1:n.*249_*251delinsATT
ENST00000700023.1:n.2068_2070delinsATT
ENST00000700024.1:n.2302_2304delinsATT
ENST00000700025.1:n.1679_1681delinsATT
ENST00000700026.1:n.547_549delinsATT
ENST00000706954.1:c.910_912delinsATT	ENSP00000516674.1:p.Cys304Ile
ENST00000706955.1:c.*945_*947delinsATT	ENSP00000516675.1:n.*945_*947delinsATT
ENST00000686459.1:c.*496_*498delinsATT	ENSP00000508909.1:n.*496_*498delinsATT
ENST00000688158.1:c.*1021_*1023delinsATT	ENSP00000509254.1:n.*1021_*1023delinsATT
ENST00000688308.1:c.910_912delinsATT	ENSP00000508752.1:p.Cys304Ile
ENST00000688922.1:c.831_833delinsATT
ENST00000693560.1:c.1429_1431delinsATT	ENSP00000509861.1:p.Cys477Ile
ENST00000371953.8:c.910_912delinsATT MANE Select	ENSP00000361021.3:p.Cys304Ile
ENST00000371953.7:c.910_912delinsATT	ENSP00000361021.3:p.Cys304Ile
ENST00000472832.2:c.337_339delinsATT	ENSP00000483066.1:p.Cys113Ile
NM_000314.5:c.910_912delinsATT	NP_000305.3:p.Cys304Ile
NM_000314.6:c.910_912delinsATT	NP_000305.3:p.Cys304Ile
NM_001304717.2:c.1429_1431delinsATT	NP_001291646.2:p.Cys477Ile
NM_001304718.1:c.319_321delinsATT	NP_001291647.1:p.Cys107Ile
XM_006717926.2:c.865_867delinsATT	XP_006717989.1:p.Cys289Ile
XM_011539981.1:c.910_912delinsATT	XP_011538283.1:p.Cys304Ile
XM_011539982.1:c.814_816delinsATT	XP_011538284.1:p.Cys272Ile
XR_945791.1:n.1480_1482delinsATT
NM_000314.7:c.910_912delinsATT	NP_000305.3:p.Cys304Ile
NM_001304717.5:c.1429_1431delinsATT	NP_001291646.4:p.Cys477Ile
NM_001304718.2:c.319_321delinsATT	NP_001291647.1:p.Cys107Ile
NM_000314.8:c.910_912delinsATT MANE Select	NP_000305.3:p.Cys304Ile