Canonical Allele Identifier: CA891835939

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87961002_87961004delinsGCT , CM000672.2:g.87961002_87961004delinsGCT	GRCh38
NC_000010.10:g.89720759_89720761delinsGCT , CM000672.1:g.89720759_89720761delinsGCT	GRCh37
NC_000010.9:g.89710739_89710741delinsGCT	NCBI36
NG_007466.2:g.102564_102566delinsGCT , LRG_311:g.102564_102566delinsGCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.1003_1005delinsGCT	ENSP00000514759.2:p.Cys335Ala
ENST00000710265.1:c.910_912delinsGCT	ENSP00000518161.1:p.Cys304Ala
ENST00000472832.3:c.910_912delinsGCT	ENSP00000483066.2:p.Cys304Ala
ENST00000688158.2:n.1645_1647delinsGCT
ENST00000688922.2:c.*740_*742delinsGCT	ENSP00000508742.2:n.*740_*742delinsGCT
ENST00000700021.1:c.865_867delinsGCT	ENSP00000514757.1:p.Cys289Ala
ENST00000700022.1:c.*249_*251delinsGCT	ENSP00000514758.1:n.*249_*251delinsGCT
ENST00000700023.1:n.2068_2070delinsGCT
ENST00000700024.1:n.2302_2304delinsGCT
ENST00000700025.1:n.1679_1681delinsGCT
ENST00000700026.1:n.547_549delinsGCT
ENST00000706954.1:c.910_912delinsGCT	ENSP00000516674.1:p.Cys304Ala
ENST00000706955.1:c.*945_*947delinsGCT	ENSP00000516675.1:n.*945_*947delinsGCT
ENST00000686459.1:c.*496_*498delinsGCT	ENSP00000508909.1:n.*496_*498delinsGCT
ENST00000688158.1:c.*1021_*1023delinsGCT	ENSP00000509254.1:n.*1021_*1023delinsGCT
ENST00000688308.1:c.910_912delinsGCT	ENSP00000508752.1:p.Cys304Ala
ENST00000688922.1:c.831_833delinsGCT
ENST00000693560.1:c.1429_1431delinsGCT	ENSP00000509861.1:p.Cys477Ala
ENST00000371953.8:c.910_912delinsGCT MANE Select	ENSP00000361021.3:p.Cys304Ala
ENST00000371953.7:c.910_912delinsGCT	ENSP00000361021.3:p.Cys304Ala
ENST00000472832.2:c.337_339delinsGCT	ENSP00000483066.1:p.Cys113Ala
NM_000314.5:c.910_912delinsGCT	NP_000305.3:p.Cys304Ala
NM_000314.6:c.910_912delinsGCT	NP_000305.3:p.Cys304Ala
NM_001304717.2:c.1429_1431delinsGCT	NP_001291646.2:p.Cys477Ala
NM_001304718.1:c.319_321delinsGCT	NP_001291647.1:p.Cys107Ala
XM_006717926.2:c.865_867delinsGCT	XP_006717989.1:p.Cys289Ala
XM_011539981.1:c.910_912delinsGCT	XP_011538283.1:p.Cys304Ala
XM_011539982.1:c.814_816delinsGCT	XP_011538284.1:p.Cys272Ala
XR_945791.1:n.1480_1482delinsGCT
NM_000314.7:c.910_912delinsGCT	NP_000305.3:p.Cys304Ala
NM_001304717.5:c.1429_1431delinsGCT	NP_001291646.4:p.Cys477Ala
NM_001304718.2:c.319_321delinsGCT	NP_001291647.1:p.Cys107Ala
NM_000314.8:c.910_912delinsGCT MANE Select	NP_000305.3:p.Cys304Ala