Canonical Allele Identifier: CA891835924

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87961002_87961004delinsAAT , CM000672.2:g.87961002_87961004delinsAAT	GRCh38
NC_000010.10:g.89720759_89720761delinsAAT , CM000672.1:g.89720759_89720761delinsAAT	GRCh37
NC_000010.9:g.89710739_89710741delinsAAT	NCBI36
NG_007466.2:g.102564_102566delinsAAT , LRG_311:g.102564_102566delinsAAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.1003_1005delinsAAT	ENSP00000514759.2:p.Cys335Asn
ENST00000710265.1:c.910_912delinsAAT	ENSP00000518161.1:p.Cys304Asn
ENST00000472832.3:c.910_912delinsAAT	ENSP00000483066.2:p.Cys304Asn
ENST00000688158.2:n.1645_1647delinsAAT
ENST00000688922.2:c.*740_*742delinsAAT	ENSP00000508742.2:n.*740_*742delinsAAT
ENST00000700021.1:c.865_867delinsAAT	ENSP00000514757.1:p.Cys289Asn
ENST00000700022.1:c.*249_*251delinsAAT	ENSP00000514758.1:n.*249_*251delinsAAT
ENST00000700023.1:n.2068_2070delinsAAT
ENST00000700024.1:n.2302_2304delinsAAT
ENST00000700025.1:n.1679_1681delinsAAT
ENST00000700026.1:n.547_549delinsAAT
ENST00000706954.1:c.910_912delinsAAT	ENSP00000516674.1:p.Cys304Asn
ENST00000706955.1:c.*945_*947delinsAAT	ENSP00000516675.1:n.*945_*947delinsAAT
ENST00000686459.1:c.*496_*498delinsAAT	ENSP00000508909.1:n.*496_*498delinsAAT
ENST00000688158.1:c.*1021_*1023delinsAAT	ENSP00000509254.1:n.*1021_*1023delinsAAT
ENST00000688308.1:c.910_912delinsAAT	ENSP00000508752.1:p.Cys304Asn
ENST00000688922.1:c.831_833delinsAAT
ENST00000693560.1:c.1429_1431delinsAAT	ENSP00000509861.1:p.Cys477Asn
ENST00000371953.8:c.910_912delinsAAT MANE Select	ENSP00000361021.3:p.Cys304Asn
ENST00000371953.7:c.910_912delinsAAT	ENSP00000361021.3:p.Cys304Asn
ENST00000472832.2:c.337_339delinsAAT	ENSP00000483066.1:p.Cys113Asn
NM_000314.5:c.910_912delinsAAT	NP_000305.3:p.Cys304Asn
NM_000314.6:c.910_912delinsAAT	NP_000305.3:p.Cys304Asn
NM_001304717.2:c.1429_1431delinsAAT	NP_001291646.2:p.Cys477Asn
NM_001304718.1:c.319_321delinsAAT	NP_001291647.1:p.Cys107Asn
XM_006717926.2:c.865_867delinsAAT	XP_006717989.1:p.Cys289Asn
XM_011539981.1:c.910_912delinsAAT	XP_011538283.1:p.Cys304Asn
XM_011539982.1:c.814_816delinsAAT	XP_011538284.1:p.Cys272Asn
XR_945791.1:n.1480_1482delinsAAT
NM_000314.7:c.910_912delinsAAT	NP_000305.3:p.Cys304Asn
NM_001304717.5:c.1429_1431delinsAAT	NP_001291646.4:p.Cys477Asn
NM_001304718.2:c.319_321delinsAAT	NP_001291647.1:p.Cys107Asn
NM_000314.8:c.910_912delinsAAT MANE Select	NP_000305.3:p.Cys304Asn