Canonical Allele Identifier: CA645553743

Gene: PTEN

Linked Data

• COSMIC: COSM4926

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87925513_87925529del , CM000672.2:g.87925513_87925529del	GRCh38
NC_000010.10:g.89685270_89685286del , CM000672.1:g.89685270_89685286del	GRCh37
NC_000010.9:g.89675250_89675266del	NCBI36
NG_007466.2:g.67075_67091del , LRG_311:g.67075_67091del

Transcript Alleles

HGVS	Amino-acid change
ENST00000700029.2:c.165_181del	ENSP00000514759.2:p.Phe56Ter
ENST00000710265.1:c.165_181del	ENSP00000518161.1:p.Phe56Ter
ENST00000472832.3:c.165_181del	ENSP00000483066.2:p.Phe56Ter
ENST00000688158.2:n.900_916del
ENST00000688922.2:c.165_181del	ENSP00000508742.2:p.Phe56Ter
ENST00000700021.1:c.165-5533_165-5517del	ENSP00000514757.1:n.165-5533_165-5517del
ENST00000700022.1:c.165_181del	ENSP00000514758.1:p.Phe56Ter
ENST00000706954.1:c.165_181del	ENSP00000516674.1:p.Phe56Ter
ENST00000706955.1:c.*200_*216del	ENSP00000516675.1:n.*200_*216del
ENST00000686459.1:c.165_181del	ENSP00000508909.1:p.Phe56Ter
ENST00000688158.1:c.*276_*292del	ENSP00000509254.1:n.*276_*292del
ENST00000688308.1:c.165_181del	ENSP00000508752.1:p.Phe56Ter
ENST00000688922.1:c.34_50del
ENST00000693560.1:c.684_700del	ENSP00000509861.1:p.Phe229Ter
ENST00000371953.8:c.165_181del MANE Select	ENSP00000361021.3:p.Phe56Ter
ENST00000371953.7:c.165_181del	ENSP00000361021.3:p.Phe56Ter
ENST00000610634.1:c.63_79del	ENSP00000477517.1:p.Phe22Ter
NM_000314.5:c.165_181del	NP_000305.3:p.Phe56Ter
NM_000314.6:c.165_181del	NP_000305.3:p.Phe56Ter
NM_001304717.2:c.684_700del	NP_001291646.2:p.Phe229Ter
NM_001304718.1:c.-541-5533_-541-5517del	NP_001291647.1:n.-541-5533_-541-5517del
XM_006717926.2:c.165-5533_165-5517del	XP_006717989.1:n.165-5533_165-5517del
XM_011539981.1:c.165_181del	XP_011538283.1:p.Phe56Ter
XM_011539982.1:c.69_85del	XP_011538284.1:p.Phe24Ter
XR_945789.1:n.877_893del
XR_945790.1:n.877_893del
XR_945791.1:n.877_893del
NM_000314.7:c.165_181del	NP_000305.3:p.Phe56Ter
NM_001304717.5:c.684_700del	NP_001291646.4:p.Phe229Ter
NM_001304718.2:c.-541-5533_-541-5517del	NP_001291647.1:n.-541-5533_-541-5517del
NM_000314.8:c.165_181del MANE Select	NP_000305.3:p.Phe56Ter