Canonical Allele Identifier: CA891841069

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87960945_87960946delinsAC , CM000672.2:g.87960945_87960946delinsAC	GRCh38
NC_000010.10:g.89720702_89720703delinsAC , CM000672.1:g.89720702_89720703delinsAC	GRCh37
NC_000010.9:g.89710682_89710683delinsAC	NCBI36
NG_007466.2:g.102507_102508delinsAC , LRG_311:g.102507_102508delinsAC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.946_947delinsAC	ENSP00000514759.2:p.Glu316Thr
ENST00000710265.1:c.853_854delinsAC	ENSP00000518161.1:p.Glu285Thr
ENST00000472832.3:c.853_854delinsAC	ENSP00000483066.2:p.Glu285Thr
ENST00000688158.2:n.1588_1589delinsAC
ENST00000688922.2:c.*683_*684delinsAC	ENSP00000508742.2:n.*683_*684delinsAC
ENST00000700021.1:c.808_809delinsAC	ENSP00000514757.1:p.Glu270Thr
ENST00000700022.1:c.*192_*193delinsAC	ENSP00000514758.1:n.*192_*193delinsAC
ENST00000700023.1:n.2011_2012delinsAC
ENST00000700024.1:n.2245_2246delinsAC
ENST00000700025.1:n.1622_1623delinsAC
ENST00000700026.1:n.490_491delinsAC
ENST00000700029.1:c.780_781delinsAC
ENST00000706954.1:c.853_854delinsAC	ENSP00000516674.1:p.Glu285Thr
ENST00000706955.1:c.*888_*889delinsAC	ENSP00000516675.1:n.*888_*889delinsAC
ENST00000686459.1:c.*439_*440delinsAC	ENSP00000508909.1:n.*439_*440delinsAC
ENST00000688158.1:c.*964_*965delinsAC	ENSP00000509254.1:n.*964_*965delinsAC
ENST00000688308.1:c.853_854delinsAC	ENSP00000508752.1:p.Glu285Thr
ENST00000688922.1:c.774_775delinsAC
ENST00000693560.1:c.1372_1373delinsAC	ENSP00000509861.1:p.Glu458Thr
ENST00000371953.8:c.853_854delinsAC MANE Select	ENSP00000361021.3:p.Glu285Thr
ENST00000371953.7:c.853_854delinsAC	ENSP00000361021.3:p.Glu285Thr
ENST00000472832.2:c.280_281delinsAC	ENSP00000483066.1:p.Glu94Thr
NM_000314.5:c.853_854delinsAC	NP_000305.3:p.Glu285Thr
NM_000314.6:c.853_854delinsAC	NP_000305.3:p.Glu285Thr
NM_001304717.2:c.1372_1373delinsAC	NP_001291646.2:p.Glu458Thr
NM_001304718.1:c.262_263delinsAC	NP_001291647.1:p.Glu88Thr
XM_006717926.2:c.808_809delinsAC	XP_006717989.1:p.Glu270Thr
XM_011539981.1:c.853_854delinsAC	XP_011538283.1:p.Glu285Thr
XM_011539982.1:c.757_758delinsAC	XP_011538284.1:p.Glu253Thr
XR_945791.1:n.1423_1424delinsAC
NM_000314.7:c.853_854delinsAC	NP_000305.3:p.Glu285Thr
NM_001304717.5:c.1372_1373delinsAC	NP_001291646.4:p.Glu458Thr
NM_001304718.2:c.262_263delinsAC	NP_001291647.1:p.Glu88Thr
NM_000314.8:c.853_854delinsAC MANE Select	NP_000305.3:p.Glu285Thr