Canonical Allele Identifier: CA891835078

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87960951_87960953delinsGAT , CM000672.2:g.87960951_87960953delinsGAT	GRCh38
NC_000010.10:g.89720708_89720710delinsGAT , CM000672.1:g.89720708_89720710delinsGAT	GRCh37
NC_000010.9:g.89710688_89710690delinsGAT	NCBI36
NG_007466.2:g.102513_102515delinsGAT , LRG_311:g.102513_102515delinsGAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.952_954delinsGAT	ENSP00000514759.2:p.Ser318Asp
ENST00000710265.1:c.859_861delinsGAT	ENSP00000518161.1:p.Ser287Asp
ENST00000472832.3:c.859_861delinsGAT	ENSP00000483066.2:p.Ser287Asp
ENST00000688158.2:n.1594_1596delinsGAT
ENST00000688922.2:c.*689_*691delinsGAT	ENSP00000508742.2:n.*689_*691delinsGAT
ENST00000700021.1:c.814_816delinsGAT	ENSP00000514757.1:p.Ser272Asp
ENST00000700022.1:c.*198_*200delinsGAT	ENSP00000514758.1:n.*198_*200delinsGAT
ENST00000700023.1:n.2017_2019delinsGAT
ENST00000700024.1:n.2251_2253delinsGAT
ENST00000700025.1:n.1628_1630delinsGAT
ENST00000700026.1:n.496_498delinsGAT
ENST00000700029.1:c.786_788delinsGAT
ENST00000706954.1:c.859_861delinsGAT	ENSP00000516674.1:p.Ser287Asp
ENST00000706955.1:c.*894_*896delinsGAT	ENSP00000516675.1:n.*894_*896delinsGAT
ENST00000686459.1:c.*445_*447delinsGAT	ENSP00000508909.1:n.*445_*447delinsGAT
ENST00000688158.1:c.*970_*972delinsGAT	ENSP00000509254.1:n.*970_*972delinsGAT
ENST00000688308.1:c.859_861delinsGAT	ENSP00000508752.1:p.Ser287Asp
ENST00000688922.1:c.780_782delinsGAT
ENST00000693560.1:c.1378_1380delinsGAT	ENSP00000509861.1:p.Ser460Asp
ENST00000371953.8:c.859_861delinsGAT MANE Select	ENSP00000361021.3:p.Ser287Asp
ENST00000371953.7:c.859_861delinsGAT	ENSP00000361021.3:p.Ser287Asp
ENST00000472832.2:c.286_288delinsGAT	ENSP00000483066.1:p.Ser96Asp
NM_000314.5:c.859_861delinsGAT	NP_000305.3:p.Ser287Asp
NM_000314.6:c.859_861delinsGAT	NP_000305.3:p.Ser287Asp
NM_001304717.2:c.1378_1380delinsGAT	NP_001291646.2:p.Ser460Asp
NM_001304718.1:c.268_270delinsGAT	NP_001291647.1:p.Ser90Asp
XM_006717926.2:c.814_816delinsGAT	XP_006717989.1:p.Ser272Asp
XM_011539981.1:c.859_861delinsGAT	XP_011538283.1:p.Ser287Asp
XM_011539982.1:c.763_765delinsGAT	XP_011538284.1:p.Ser255Asp
XR_945791.1:n.1429_1431delinsGAT
NM_000314.7:c.859_861delinsGAT	NP_000305.3:p.Ser287Asp
NM_001304717.5:c.1378_1380delinsGAT	NP_001291646.4:p.Ser460Asp
NM_001304718.2:c.268_270delinsGAT	NP_001291647.1:p.Ser90Asp
NM_000314.8:c.859_861delinsGAT MANE Select	NP_000305.3:p.Ser287Asp