Canonical Allele Identifier: CA645545320

Gene: PTEN

Linked Data

• COSMIC: COSM2156793

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87965373del , CM000672.2:g.87965373del	GRCh38
NC_000010.10:g.89725130del , CM000672.1:g.89725130del	GRCh37
NC_000010.9:g.89715110del	NCBI36
NG_007466.2:g.106935del , LRG_311:g.106935del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.1206del	ENSP00000514759.2:p.Asp402GlufsTer?
ENST00000710265.1:c.*142del	ENSP00000518161.1:n.*142del
ENST00000688158.2:n.1848del
ENST00000688922.2:c.*943del	ENSP00000508742.2:n.*943del
ENST00000700021.1:c.1068del	ENSP00000514757.1:p.Asp356GlufsTer?
ENST00000700022.1:c.*452del	ENSP00000514758.1:n.*452del
ENST00000700023.1:n.2271del
ENST00000700024.1:n.2505del
ENST00000706954.1:c.1113del	ENSP00000516674.1:p.Asp371GlufsTer?
ENST00000706955.1:c.*1148del	ENSP00000516675.1:n.*1148del
ENST00000686459.1:c.*699del	ENSP00000508909.1:n.*699del
ENST00000688158.1:c.*1224del	ENSP00000509254.1:n.*1224del
ENST00000688308.1:c.1113del	ENSP00000508752.1:p.Asp371GlufsTer?
ENST00000688922.1:c.1034del
ENST00000693560.1:c.1632del	ENSP00000509861.1:p.Asp544GlufsTer?
ENST00000371953.8:c.1113del MANE Select	ENSP00000361021.3:p.Asp371GlufsTer?
ENST00000371953.7:c.1113del	ENSP00000361021.3:p.Asp371GlufsTer?
NM_000314.5:c.1113del	NP_000305.3:p.Asp371GlufsTer?
NM_000314.6:c.1113del	NP_000305.3:p.Asp371GlufsTer?
NM_001304717.2:c.1632del	NP_001291646.2:p.Asp544GlufsTer?
NM_001304718.1:c.522del	NP_001291647.1:p.Asp174GlufsTer?
XM_006717926.2:c.1068del	XP_006717989.1:p.Asp356GlufsTer?
XM_011539982.1:c.1017del	XP_011538284.1:p.Asp339GlufsTer?
XR_945791.1:n.1683del
NM_000314.7:c.1113del	NP_000305.3:p.Asp371GlufsTer?
NM_001304717.5:c.1632del	NP_001291646.4:p.Asp544GlufsTer?
NM_001304718.2:c.522del	NP_001291647.1:p.Asp174GlufsTer?
NM_000314.8:c.1113del MANE Select	NP_000305.3:p.Asp371GlufsTer?