Canonical Allele Identifier: CA645553798

Gene: PTEN

Linked Data

• COSMIC: COSM4944

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87933038_87933063del , CM000672.2:g.87933038_87933063del	GRCh38
NC_000010.10:g.89692795_89692820del , CM000672.1:g.89692795_89692820del	GRCh37
NC_000010.9:g.89682775_89682800del	NCBI36
NG_007466.2:g.74600_74625del , LRG_311:g.74600_74625del

Transcript Alleles

HGVS	Amino-acid change
ENST00000700029.2:c.279_304del	ENSP00000514759.2:p.His93GlnfsTer5
ENST00000710265.1:c.279_304del	ENSP00000518161.1:p.His93GlnfsTer5
ENST00000472832.3:c.279_304del	ENSP00000483066.2:p.His93GlnfsTer5
ENST00000688158.2:n.1014_1039del
ENST00000688922.2:c.*109_*134del	ENSP00000508742.2:n.*109_*134del
ENST00000700021.1:c.234_259del	ENSP00000514757.1:p.His78GlnfsTer5
ENST00000700022.1:c.279_304del	ENSP00000514758.1:p.His93GlnfsTer5
ENST00000700029.1:c.113_138del
ENST00000706954.1:c.279_304del	ENSP00000516674.1:p.His93GlnfsTer5
ENST00000706955.1:c.*314_*339del	ENSP00000516675.1:n.*314_*339del
ENST00000686459.1:c.279_304del	ENSP00000508909.1:p.His93GlnfsTer5
ENST00000688158.1:c.*390_*415del	ENSP00000509254.1:n.*390_*415del
ENST00000688308.1:c.279_304del	ENSP00000508752.1:p.His93GlnfsTer5
ENST00000688922.1:c.200_225del
ENST00000693560.1:c.798_823del	ENSP00000509861.1:p.His266GlnfsTer5
ENST00000371953.8:c.279_304del MANE Select	ENSP00000361021.3:p.His93GlnfsTer5
ENST00000371953.7:c.279_304del	ENSP00000361021.3:p.His93GlnfsTer5
ENST00000498703.1:n.105_130del
ENST00000610634.1:c.177_202del	ENSP00000477517.1:p.His59GlnfsTer5
NM_000314.5:c.279_304del	NP_000305.3:p.His93GlnfsTer5
NM_000314.6:c.279_304del	NP_000305.3:p.His93GlnfsTer5
NM_001304717.2:c.798_823del	NP_001291646.2:p.His266GlnfsTer5
NM_001304718.1:c.-472_-447del	NP_001291647.1:n.-472_-447del
XM_006717926.2:c.234_259del	XP_006717989.1:p.His78GlnfsTer5
XM_011539981.1:c.279_304del	XP_011538283.1:p.His93GlnfsTer5
XM_011539982.1:c.183_208del	XP_011538284.1:p.His61GlnfsTer5
XR_945789.1:n.991_1016del
XR_945790.1:n.991_1016del
XR_945791.1:n.991_1016del
NM_000314.7:c.279_304del	NP_000305.3:p.His93GlnfsTer5
NM_001304717.5:c.798_823del	NP_001291646.4:p.His266GlnfsTer5
NM_001304718.2:c.-472_-447del	NP_001291647.1:n.-472_-447del
NM_000314.8:c.279_304del MANE Select	NP_000305.3:p.His93GlnfsTer5