Canonical Allele Identifier: CA891835086

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87960951_87960953delinsGTT , CM000672.2:g.87960951_87960953delinsGTT	GRCh38
NC_000010.10:g.89720708_89720710delinsGTT , CM000672.1:g.89720708_89720710delinsGTT	GRCh37
NC_000010.9:g.89710688_89710690delinsGTT	NCBI36
NG_007466.2:g.102513_102515delinsGTT , LRG_311:g.102513_102515delinsGTT

Transcript Alleles

HGVS	Amino-acid change
ENST00000700029.2:c.952_954delinsGTT	ENSP00000514759.2:p.Ser318Val
ENST00000710265.1:c.859_861delinsGTT	ENSP00000518161.1:p.Ser287Val
ENST00000472832.3:c.859_861delinsGTT	ENSP00000483066.2:p.Ser287Val
ENST00000688158.2:n.1594_1596delinsGTT
ENST00000688922.2:c.*689_*691delinsGTT	ENSP00000508742.2:n.*689_*691delinsGTT
ENST00000700021.1:c.814_816delinsGTT	ENSP00000514757.1:p.Ser272Val
ENST00000700022.1:c.*198_*200delinsGTT	ENSP00000514758.1:n.*198_*200delinsGTT
ENST00000700023.1:n.2017_2019delinsGTT
ENST00000700024.1:n.2251_2253delinsGTT
ENST00000700025.1:n.1628_1630delinsGTT
ENST00000700026.1:n.496_498delinsGTT
ENST00000700029.1:c.786_788delinsGTT
ENST00000706954.1:c.859_861delinsGTT	ENSP00000516674.1:p.Ser287Val
ENST00000706955.1:c.*894_*896delinsGTT	ENSP00000516675.1:n.*894_*896delinsGTT
ENST00000686459.1:c.*445_*447delinsGTT	ENSP00000508909.1:n.*445_*447delinsGTT
ENST00000688158.1:c.*970_*972delinsGTT	ENSP00000509254.1:n.*970_*972delinsGTT
ENST00000688308.1:c.859_861delinsGTT	ENSP00000508752.1:p.Ser287Val
ENST00000688922.1:c.780_782delinsGTT
ENST00000693560.1:c.1378_1380delinsGTT	ENSP00000509861.1:p.Ser460Val
ENST00000371953.8:c.859_861delinsGTT MANE Select	ENSP00000361021.3:p.Ser287Val
ENST00000371953.7:c.859_861delinsGTT	ENSP00000361021.3:p.Ser287Val
ENST00000472832.2:c.286_288delinsGTT	ENSP00000483066.1:p.Ser96Val
NM_000314.5:c.859_861delinsGTT	NP_000305.3:p.Ser287Val
NM_000314.6:c.859_861delinsGTT	NP_000305.3:p.Ser287Val
NM_001304717.2:c.1378_1380delinsGTT	NP_001291646.2:p.Ser460Val
NM_001304718.1:c.268_270delinsGTT	NP_001291647.1:p.Ser90Val
XM_006717926.2:c.814_816delinsGTT	XP_006717989.1:p.Ser272Val
XM_011539981.1:c.859_861delinsGTT	XP_011538283.1:p.Ser287Val
XM_011539982.1:c.763_765delinsGTT	XP_011538284.1:p.Ser255Val
XR_945791.1:n.1429_1431delinsGTT
NM_000314.7:c.859_861delinsGTT	NP_000305.3:p.Ser287Val
NM_001304717.5:c.1378_1380delinsGTT	NP_001291646.4:p.Ser460Val
NM_001304718.2:c.268_270delinsGTT	NP_001291647.1:p.Ser90Val
NM_000314.8:c.859_861delinsGTT MANE Select	NP_000305.3:p.Ser287Val