Canonical Allele Identifier: CA2579926797

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87960903_87960905del , CM000672.2:g.87960903_87960905del	GRCh38
NC_000010.10:g.89720660_89720662del , CM000672.1:g.89720660_89720662del	GRCh37
NC_000010.9:g.89710640_89710642del	NCBI36
NG_007466.2:g.102465_102467del , LRG_311:g.102465_102467del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.904_906del	ENSP00000514759.2:p.Phe302del
ENST00000710265.1:c.811_813del	ENSP00000518161.1:p.Phe271del
ENST00000472832.3:c.811_813del	ENSP00000483066.2:p.Phe271del
ENST00000688158.2:n.1546_1548del
ENST00000688922.2:c.*641_*643del	ENSP00000508742.2:n.*641_*643del
ENST00000700021.1:c.766_768del	ENSP00000514757.1:p.Phe256del
ENST00000700022.1:c.*150_*152del	ENSP00000514758.1:n.*150_*152del
ENST00000700023.1:n.1969_1971del
ENST00000700024.1:n.2203_2205del
ENST00000700025.1:n.1580_1582del
ENST00000700026.1:n.448_450del
ENST00000700029.1:c.738_740del
ENST00000706954.1:c.811_813del	ENSP00000516674.1:p.Phe271del
ENST00000706955.1:c.*846_*848del	ENSP00000516675.1:n.*846_*848del
ENST00000686459.1:c.*397_*399del	ENSP00000508909.1:n.*397_*399del
ENST00000688158.1:c.*922_*924del	ENSP00000509254.1:n.*922_*924del
ENST00000688308.1:c.811_813del	ENSP00000508752.1:p.Phe271del
ENST00000688922.1:c.732_734del
ENST00000693560.1:c.1330_1332del	ENSP00000509861.1:p.Phe444del
ENST00000371953.8:c.811_813del MANE Select	ENSP00000361021.3:p.Phe271del
ENST00000371953.7:c.811_813del	ENSP00000361021.3:p.Phe271del
ENST00000472832.2:c.238_240del	ENSP00000483066.1:p.Phe80del
NM_000314.5:c.811_813del	NP_000305.3:p.Phe271del
NM_000314.6:c.811_813del	NP_000305.3:p.Phe271del
NM_001304717.2:c.1330_1332del	NP_001291646.2:p.Phe444del
NM_001304718.1:c.220_222del	NP_001291647.1:p.Phe74del
XM_006717926.2:c.766_768del	XP_006717989.1:p.Phe256del
XM_011539981.1:c.811_813del	XP_011538283.1:p.Phe271del
XM_011539982.1:c.715_717del	XP_011538284.1:p.Phe239del
XR_945791.1:n.1381_1383del
NM_000314.7:c.811_813del	NP_000305.3:p.Phe271del
NM_001304717.5:c.1330_1332del	NP_001291646.4:p.Phe444del
NM_001304718.2:c.220_222del	NP_001291647.1:p.Phe74del
NM_000314.8:c.811_813del MANE Select	NP_000305.3:p.Phe271del