Canonical Allele Identifier: CA913189220

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87965356del , CM000672.2:g.87965356del	GRCh38
NC_000010.10:g.89725113del , CM000672.1:g.89725113del	GRCh37
NC_000010.9:g.89715093del	NCBI36
NG_007466.2:g.106918del , LRG_311:g.106918del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.1189del	ENSP00000514759.2:p.Thr397HisfsTer?
ENST00000710265.1:c.*125del	ENSP00000518161.1:n.*125del
ENST00000688158.2:n.1831del
ENST00000688922.2:c.*926del	ENSP00000508742.2:n.*926del
ENST00000700021.1:c.1051del	ENSP00000514757.1:p.Thr351HisfsTer?
ENST00000700022.1:c.*435del	ENSP00000514758.1:n.*435del
ENST00000700023.1:n.2254del
ENST00000700024.1:n.2488del
ENST00000706954.1:c.1096del	ENSP00000516674.1:p.Thr366HisfsTer?
ENST00000706955.1:c.*1131del	ENSP00000516675.1:n.*1131del
ENST00000686459.1:c.*682del	ENSP00000508909.1:n.*682del
ENST00000688158.1:c.*1207del	ENSP00000509254.1:n.*1207del
ENST00000688308.1:c.1096del	ENSP00000508752.1:p.Thr366HisfsTer?
ENST00000688922.1:c.1017del
ENST00000693560.1:c.1615del	ENSP00000509861.1:p.Thr539HisfsTer?
ENST00000371953.8:c.1096del MANE Select	ENSP00000361021.3:p.Thr366HisfsTer?
ENST00000371953.7:c.1096del	ENSP00000361021.3:p.Thr366HisfsTer?
NM_000314.5:c.1096del	NP_000305.3:p.Thr366HisfsTer?
NM_000314.6:c.1096del	NP_000305.3:p.Thr366HisfsTer?
NM_001304717.2:c.1615del	NP_001291646.2:p.Thr539HisfsTer?
NM_001304718.1:c.505del	NP_001291647.1:p.Thr169HisfsTer?
XM_006717926.2:c.1051del	XP_006717989.1:p.Thr351HisfsTer?
XM_011539982.1:c.1000del	XP_011538284.1:p.Thr334HisfsTer?
XR_945791.1:n.1666del
NM_000314.7:c.1096del	NP_000305.3:p.Thr366HisfsTer?
NM_001304717.5:c.1615del	NP_001291646.4:p.Thr539HisfsTer?
NM_001304718.2:c.505del	NP_001291647.1:p.Thr169HisfsTer?
NM_000314.8:c.1096del MANE Select	NP_000305.3:p.Thr366HisfsTer?