Canonical Allele Identifier: CA2579986008

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87965434_87965436del , CM000672.2:g.87965434_87965436del	GRCh38
NC_000010.10:g.89725191_89725193del , CM000672.1:g.89725191_89725193del	GRCh37
NC_000010.9:g.89715171_89715173del	NCBI36
NG_007466.2:g.106996_106998del , LRG_311:g.106996_106998del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.1267_1269del	ENSP00000514759.2:p.Phe423del
ENST00000710265.1:c.*203_*205del	ENSP00000518161.1:n.*203_*205del
ENST00000688158.2:n.1909_1911del
ENST00000688922.2:c.*1004_*1006del	ENSP00000508742.2:n.*1004_*1006del
ENST00000700021.1:c.1129_1131del	ENSP00000514757.1:p.Phe377del
ENST00000700022.1:c.*513_*515del	ENSP00000514758.1:n.*513_*515del
ENST00000700023.1:n.2332_2334del
ENST00000700024.1:n.2566_2568del
ENST00000706954.1:c.1174_1176del	ENSP00000516674.1:p.Phe392del
ENST00000706955.1:c.*1209_*1211del	ENSP00000516675.1:n.*1209_*1211del
ENST00000686459.1:c.*760_*762del	ENSP00000508909.1:n.*760_*762del
ENST00000688158.1:c.*1285_*1287del	ENSP00000509254.1:n.*1285_*1287del
ENST00000688308.1:c.1174_1176del	ENSP00000508752.1:p.Phe392del
ENST00000688922.1:c.1095_1097del
ENST00000693560.1:c.1693_1695del	ENSP00000509861.1:p.Phe565del
ENST00000371953.8:c.1174_1176del MANE Select	ENSP00000361021.3:p.Phe392del
ENST00000371953.7:c.1174_1176del	ENSP00000361021.3:p.Phe392del
NM_000314.5:c.1174_1176del	NP_000305.3:p.Phe392del
NM_000314.6:c.1174_1176del	NP_000305.3:p.Phe392del
NM_001304717.2:c.1693_1695del	NP_001291646.2:p.Phe565del
NM_001304718.1:c.583_585del	NP_001291647.1:p.Phe195del
XM_006717926.2:c.1129_1131del	XP_006717989.1:p.Phe377del
XM_011539982.1:c.1078_1080del	XP_011538284.1:p.Phe360del
XR_945791.1:n.1744_1746del
NM_000314.7:c.1174_1176del	NP_000305.3:p.Phe392del
NM_001304717.5:c.1693_1695del	NP_001291646.4:p.Phe565del
NM_001304718.2:c.583_585del	NP_001291647.1:p.Phe195del
NM_000314.8:c.1174_1176del MANE Select	NP_000305.3:p.Phe392del