Canonical Allele Identifier: CA891835930

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87961002_87961004delinsGAT , CM000672.2:g.87961002_87961004delinsGAT	GRCh38
NC_000010.10:g.89720759_89720761delinsGAT , CM000672.1:g.89720759_89720761delinsGAT	GRCh37
NC_000010.9:g.89710739_89710741delinsGAT	NCBI36
NG_007466.2:g.102564_102566delinsGAT , LRG_311:g.102564_102566delinsGAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.1003_1005delinsGAT	ENSP00000514759.2:p.Cys335Asp
ENST00000710265.1:c.910_912delinsGAT	ENSP00000518161.1:p.Cys304Asp
ENST00000472832.3:c.910_912delinsGAT	ENSP00000483066.2:p.Cys304Asp
ENST00000688158.2:n.1645_1647delinsGAT
ENST00000688922.2:c.*740_*742delinsGAT	ENSP00000508742.2:n.*740_*742delinsGAT
ENST00000700021.1:c.865_867delinsGAT	ENSP00000514757.1:p.Cys289Asp
ENST00000700022.1:c.*249_*251delinsGAT	ENSP00000514758.1:n.*249_*251delinsGAT
ENST00000700023.1:n.2068_2070delinsGAT
ENST00000700024.1:n.2302_2304delinsGAT
ENST00000700025.1:n.1679_1681delinsGAT
ENST00000700026.1:n.547_549delinsGAT
ENST00000706954.1:c.910_912delinsGAT	ENSP00000516674.1:p.Cys304Asp
ENST00000706955.1:c.*945_*947delinsGAT	ENSP00000516675.1:n.*945_*947delinsGAT
ENST00000686459.1:c.*496_*498delinsGAT	ENSP00000508909.1:n.*496_*498delinsGAT
ENST00000688158.1:c.*1021_*1023delinsGAT	ENSP00000509254.1:n.*1021_*1023delinsGAT
ENST00000688308.1:c.910_912delinsGAT	ENSP00000508752.1:p.Cys304Asp
ENST00000688922.1:c.831_833delinsGAT
ENST00000693560.1:c.1429_1431delinsGAT	ENSP00000509861.1:p.Cys477Asp
ENST00000371953.8:c.910_912delinsGAT MANE Select	ENSP00000361021.3:p.Cys304Asp
ENST00000371953.7:c.910_912delinsGAT	ENSP00000361021.3:p.Cys304Asp
ENST00000472832.2:c.337_339delinsGAT	ENSP00000483066.1:p.Cys113Asp
NM_000314.5:c.910_912delinsGAT	NP_000305.3:p.Cys304Asp
NM_000314.6:c.910_912delinsGAT	NP_000305.3:p.Cys304Asp
NM_001304717.2:c.1429_1431delinsGAT	NP_001291646.2:p.Cys477Asp
NM_001304718.1:c.319_321delinsGAT	NP_001291647.1:p.Cys107Asp
XM_006717926.2:c.865_867delinsGAT	XP_006717989.1:p.Cys289Asp
XM_011539981.1:c.910_912delinsGAT	XP_011538283.1:p.Cys304Asp
XM_011539982.1:c.814_816delinsGAT	XP_011538284.1:p.Cys272Asp
XR_945791.1:n.1480_1482delinsGAT
NM_000314.7:c.910_912delinsGAT	NP_000305.3:p.Cys304Asp
NM_001304717.5:c.1429_1431delinsGAT	NP_001291646.4:p.Cys477Asp
NM_001304718.2:c.319_321delinsGAT	NP_001291647.1:p.Cys107Asp
NM_000314.8:c.910_912delinsGAT MANE Select	NP_000305.3:p.Cys304Asp