Canonical Allele Identifier: CA891835076

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87960951_87960953delinsACT , CM000672.2:g.87960951_87960953delinsACT	GRCh38
NC_000010.10:g.89720708_89720710delinsACT , CM000672.1:g.89720708_89720710delinsACT	GRCh37
NC_000010.9:g.89710688_89710690delinsACT	NCBI36
NG_007466.2:g.102513_102515delinsACT , LRG_311:g.102513_102515delinsACT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.952_954delinsACT	ENSP00000514759.2:p.Ser318Thr
ENST00000710265.1:c.859_861delinsACT	ENSP00000518161.1:p.Ser287Thr
ENST00000472832.3:c.859_861delinsACT	ENSP00000483066.2:p.Ser287Thr
ENST00000688158.2:n.1594_1596delinsACT
ENST00000688922.2:c.*689_*691delinsACT	ENSP00000508742.2:n.*689_*691delinsACT
ENST00000700021.1:c.814_816delinsACT	ENSP00000514757.1:p.Ser272Thr
ENST00000700022.1:c.*198_*200delinsACT	ENSP00000514758.1:n.*198_*200delinsACT
ENST00000700023.1:n.2017_2019delinsACT
ENST00000700024.1:n.2251_2253delinsACT
ENST00000700025.1:n.1628_1630delinsACT
ENST00000700026.1:n.496_498delinsACT
ENST00000700029.1:c.786_788delinsACT
ENST00000706954.1:c.859_861delinsACT	ENSP00000516674.1:p.Ser287Thr
ENST00000706955.1:c.*894_*896delinsACT	ENSP00000516675.1:n.*894_*896delinsACT
ENST00000686459.1:c.*445_*447delinsACT	ENSP00000508909.1:n.*445_*447delinsACT
ENST00000688158.1:c.*970_*972delinsACT	ENSP00000509254.1:n.*970_*972delinsACT
ENST00000688308.1:c.859_861delinsACT	ENSP00000508752.1:p.Ser287Thr
ENST00000688922.1:c.780_782delinsACT
ENST00000693560.1:c.1378_1380delinsACT	ENSP00000509861.1:p.Ser460Thr
ENST00000371953.8:c.859_861delinsACT MANE Select	ENSP00000361021.3:p.Ser287Thr
ENST00000371953.7:c.859_861delinsACT	ENSP00000361021.3:p.Ser287Thr
ENST00000472832.2:c.286_288delinsACT	ENSP00000483066.1:p.Ser96Thr
NM_000314.5:c.859_861delinsACT	NP_000305.3:p.Ser287Thr
NM_000314.6:c.859_861delinsACT	NP_000305.3:p.Ser287Thr
NM_001304717.2:c.1378_1380delinsACT	NP_001291646.2:p.Ser460Thr
NM_001304718.1:c.268_270delinsACT	NP_001291647.1:p.Ser90Thr
XM_006717926.2:c.814_816delinsACT	XP_006717989.1:p.Ser272Thr
XM_011539981.1:c.859_861delinsACT	XP_011538283.1:p.Ser287Thr
XM_011539982.1:c.763_765delinsACT	XP_011538284.1:p.Ser255Thr
XR_945791.1:n.1429_1431delinsACT
NM_000314.7:c.859_861delinsACT	NP_000305.3:p.Ser287Thr
NM_001304717.5:c.1378_1380delinsACT	NP_001291646.4:p.Ser460Thr
NM_001304718.2:c.268_270delinsACT	NP_001291647.1:p.Ser90Thr
NM_000314.8:c.859_861delinsACT MANE Select	NP_000305.3:p.Ser287Thr