Canonical Allele Identifier: CA891840675

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87894099_87894100delinsCT , CM000672.2:g.87894099_87894100delinsCT	GRCh38
NC_000010.10:g.89653856_89653857delinsCT , CM000672.1:g.89653856_89653857delinsCT	GRCh37
NC_000010.9:g.89643836_89643837delinsCT	NCBI36
NG_007466.2:g.35661_35662delinsCT , LRG_311:g.35661_35662delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.154_155delinsCT	ENSP00000514759.2:p.Asp52Leu
ENST00000710265.1:c.154_155delinsCT	ENSP00000518161.1:p.Asp52Leu
ENST00000472832.3:c.154_155delinsCT	ENSP00000483066.2:p.Asp52Leu
ENST00000688158.2:n.899+13661_899+13662delinsCT
ENST00000688922.2:c.154_155delinsCT	ENSP00000508742.2:p.Asp52Leu
ENST00000700021.1:c.154_155delinsCT	ENSP00000514757.1:p.Asp52Leu
ENST00000700022.1:c.154_155delinsCT	ENSP00000514758.1:p.Asp52Leu
ENST00000706954.1:c.154_155delinsCT	ENSP00000516674.1:p.Asp52Leu
ENST00000706955.1:c.*189_*190delinsCT	ENSP00000516675.1:n.*189_*190delinsCT
ENST00000686459.1:c.154_155delinsCT	ENSP00000508909.1:p.Asp52Leu
ENST00000688158.1:c.*275+13661_*275+13662delinsCT	ENSP00000509254.1:n.*275+13661_*275+13662delinsCT
ENST00000688308.1:c.154_155delinsCT	ENSP00000508752.1:p.Asp52Leu
ENST00000688922.1:c.23_24delinsCT
ENST00000693560.1:c.673_674delinsCT	ENSP00000509861.1:p.Asp225Leu
ENST00000371953.8:c.154_155delinsCT MANE Select	ENSP00000361021.3:p.Asp52Leu
ENST00000371953.7:c.154_155delinsCT	ENSP00000361021.3:p.Asp52Leu
ENST00000462694.1:n.156_157delinsCT
ENST00000610634.1:c.52_53delinsCT	ENSP00000477517.1:p.Asp18Leu
NM_000314.5:c.154_155delinsCT	NP_000305.3:p.Asp52Leu
NM_000314.6:c.154_155delinsCT	NP_000305.3:p.Asp52Leu
NM_001304717.2:c.673_674delinsCT	NP_001291646.2:p.Asp225Leu
NM_001304718.1:c.-552_-551delinsCT	NP_001291647.1:n.-552_-551delinsCT
XM_006717926.2:c.154_155delinsCT	XP_006717989.1:p.Asp52Leu
XM_011539981.1:c.154_155delinsCT	XP_011538283.1:p.Asp52Leu
XM_011539982.1:c.68+13661_68+13662delinsCT	XP_011538284.1:n.68+13661_68+13662delinsCT
XR_945789.1:n.866_867delinsCT
XR_945790.1:n.866_867delinsCT
XR_945791.1:n.866_867delinsCT
NM_000314.7:c.154_155delinsCT	NP_000305.3:p.Asp52Leu
NM_001304717.5:c.673_674delinsCT	NP_001291646.4:p.Asp225Leu
NM_001304718.2:c.-552_-551delinsCT	NP_001291647.1:n.-552_-551delinsCT
NM_000314.8:c.154_155delinsCT MANE Select	NP_000305.3:p.Asp52Leu