Canonical Allele Identifier: CA645553841

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87933163_87933168del , CM000672.2:g.87933163_87933168del	GRCh38
NC_000010.10:g.89692920_89692925del , CM000672.1:g.89692920_89692925del	GRCh37
NC_000010.9:g.89682900_89682905del	NCBI36
NG_007466.2:g.74725_74730del , LRG_311:g.74725_74730del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.404_409del	ENSP00000514759.2:p.Ile135_Ala137delinsThr
ENST00000710265.1:c.404_409del	ENSP00000518161.1:p.Ile135_Ala137delinsThr
ENST00000472832.3:c.404_409del	ENSP00000483066.2:p.Ile135_Ala137delinsThr
ENST00000688158.2:n.1139_1144del
ENST00000688922.2:c.*234_*239del	ENSP00000508742.2:n.*234_*239del
ENST00000700021.1:c.359_364del	ENSP00000514757.1:p.Ile120_Ala122delinsThr
ENST00000700022.1:c.404_409del	ENSP00000514758.1:p.Ile135_Ala137delinsThr
ENST00000700029.1:c.238_243del
ENST00000706954.1:c.404_409del	ENSP00000516674.1:p.Ile135_Ala137delinsThr
ENST00000706955.1:c.*439_*444del	ENSP00000516675.1:n.*439_*444del
ENST00000686459.1:c.404_409del	ENSP00000508909.1:p.Ile135_Ala137delinsThr
ENST00000688158.1:c.*515_*520del	ENSP00000509254.1:n.*515_*520del
ENST00000688308.1:c.404_409del	ENSP00000508752.1:p.Ile135_Ala137delinsThr
ENST00000688922.1:c.325_330del
ENST00000693560.1:c.923_928del	ENSP00000509861.1:p.Ile308_Ala310delinsThr
ENST00000371953.8:c.404_409del MANE Select	ENSP00000361021.3:p.Ile135_Ala137delinsThr
ENST00000371953.7:c.404_409del	ENSP00000361021.3:p.Ile135_Ala137delinsThr
ENST00000498703.1:n.230_235del
ENST00000610634.1:c.302_307del	ENSP00000477517.1:p.Ile101_Ala103delinsThr
NM_000314.5:c.404_409del	NP_000305.3:p.Ile135_Ala137delinsThr
NM_000314.6:c.404_409del	NP_000305.3:p.Ile135_Ala137delinsThr
NM_001304717.2:c.923_928del	NP_001291646.2:p.Ile308_Ala310delinsThr
NM_001304718.1:c.-347_-342del	NP_001291647.1:n.-347_-342del
XM_006717926.2:c.359_364del	XP_006717989.1:p.Ile120_Ala122delinsThr
XM_011539981.1:c.404_409del	XP_011538283.1:p.Ile135_Ala137delinsThr
XM_011539982.1:c.308_313del	XP_011538284.1:p.Ile103_Ala105delinsThr
XR_945789.1:n.1116_1121del
XR_945790.1:n.1116_1121del
XR_945791.1:n.1116_1121del
NM_000314.7:c.404_409del	NP_000305.3:p.Ile135_Ala137delinsThr
NM_001304717.5:c.923_928del	NP_001291646.4:p.Ile308_Ala310delinsThr
NM_001304718.2:c.-347_-342del	NP_001291647.1:n.-347_-342del
NM_000314.8:c.404_409del MANE Select	NP_000305.3:p.Ile135_Ala137delinsThr