Canonical Allele Identifier: CA891835926

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87961002_87961004delinsACT , CM000672.2:g.87961002_87961004delinsACT	GRCh38
NC_000010.10:g.89720759_89720761delinsACT , CM000672.1:g.89720759_89720761delinsACT	GRCh37
NC_000010.9:g.89710739_89710741delinsACT	NCBI36
NG_007466.2:g.102564_102566delinsACT , LRG_311:g.102564_102566delinsACT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.1003_1005delinsACT	ENSP00000514759.2:p.Cys335Thr
ENST00000710265.1:c.910_912delinsACT	ENSP00000518161.1:p.Cys304Thr
ENST00000472832.3:c.910_912delinsACT	ENSP00000483066.2:p.Cys304Thr
ENST00000688158.2:n.1645_1647delinsACT
ENST00000688922.2:c.*740_*742delinsACT	ENSP00000508742.2:n.*740_*742delinsACT
ENST00000700021.1:c.865_867delinsACT	ENSP00000514757.1:p.Cys289Thr
ENST00000700022.1:c.*249_*251delinsACT	ENSP00000514758.1:n.*249_*251delinsACT
ENST00000700023.1:n.2068_2070delinsACT
ENST00000700024.1:n.2302_2304delinsACT
ENST00000700025.1:n.1679_1681delinsACT
ENST00000700026.1:n.547_549delinsACT
ENST00000706954.1:c.910_912delinsACT	ENSP00000516674.1:p.Cys304Thr
ENST00000706955.1:c.*945_*947delinsACT	ENSP00000516675.1:n.*945_*947delinsACT
ENST00000686459.1:c.*496_*498delinsACT	ENSP00000508909.1:n.*496_*498delinsACT
ENST00000688158.1:c.*1021_*1023delinsACT	ENSP00000509254.1:n.*1021_*1023delinsACT
ENST00000688308.1:c.910_912delinsACT	ENSP00000508752.1:p.Cys304Thr
ENST00000688922.1:c.831_833delinsACT
ENST00000693560.1:c.1429_1431delinsACT	ENSP00000509861.1:p.Cys477Thr
ENST00000371953.8:c.910_912delinsACT MANE Select	ENSP00000361021.3:p.Cys304Thr
ENST00000371953.7:c.910_912delinsACT	ENSP00000361021.3:p.Cys304Thr
ENST00000472832.2:c.337_339delinsACT	ENSP00000483066.1:p.Cys113Thr
NM_000314.5:c.910_912delinsACT	NP_000305.3:p.Cys304Thr
NM_000314.6:c.910_912delinsACT	NP_000305.3:p.Cys304Thr
NM_001304717.2:c.1429_1431delinsACT	NP_001291646.2:p.Cys477Thr
NM_001304718.1:c.319_321delinsACT	NP_001291647.1:p.Cys107Thr
XM_006717926.2:c.865_867delinsACT	XP_006717989.1:p.Cys289Thr
XM_011539981.1:c.910_912delinsACT	XP_011538283.1:p.Cys304Thr
XM_011539982.1:c.814_816delinsACT	XP_011538284.1:p.Cys272Thr
XR_945791.1:n.1480_1482delinsACT
NM_000314.7:c.910_912delinsACT	NP_000305.3:p.Cys304Thr
NM_001304717.5:c.1429_1431delinsACT	NP_001291646.4:p.Cys477Thr
NM_001304718.2:c.319_321delinsACT	NP_001291647.1:p.Cys107Thr
NM_000314.8:c.910_912delinsACT MANE Select	NP_000305.3:p.Cys304Thr