Canonical Allele Identifier: CA891836902

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87961084_87961085delinsCT , CM000672.2:g.87961084_87961085delinsCT	GRCh38
NC_000010.10:g.89720841_89720842delinsCT , CM000672.1:g.89720841_89720842delinsCT	GRCh37
NC_000010.9:g.89710821_89710822delinsCT	NCBI36
NG_007466.2:g.102646_102647delinsCT , LRG_311:g.102646_102647delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.1085_1086delinsCT	ENSP00000514759.2:p.Asp362Ala
ENST00000710265.1:c.992_993delinsCT	ENSP00000518161.1:p.Asp331Ala
ENST00000472832.3:c.992_993delinsCT	ENSP00000483066.2:p.Asp331Ala
ENST00000688158.2:n.1727_1728delinsCT
ENST00000688922.2:c.*822_*823delinsCT	ENSP00000508742.2:n.*822_*823delinsCT
ENST00000700021.1:c.947_948delinsCT	ENSP00000514757.1:p.Asp316Ala
ENST00000700022.1:c.*331_*332delinsCT	ENSP00000514758.1:n.*331_*332delinsCT
ENST00000700023.1:n.2150_2151delinsCT
ENST00000700024.1:n.2384_2385delinsCT
ENST00000700025.1:n.1761_1762delinsCT
ENST00000700026.1:n.629_630delinsCT
ENST00000706954.1:c.992_993delinsCT	ENSP00000516674.1:p.Asp331Ala
ENST00000706955.1:c.*1027_*1028delinsCT	ENSP00000516675.1:n.*1027_*1028delinsCT
ENST00000686459.1:c.*578_*579delinsCT	ENSP00000508909.1:n.*578_*579delinsCT
ENST00000688158.1:c.*1103_*1104delinsCT	ENSP00000509254.1:n.*1103_*1104delinsCT
ENST00000688308.1:c.992_993delinsCT	ENSP00000508752.1:p.Asp331Ala
ENST00000688922.1:c.913_914delinsCT
ENST00000693560.1:c.1511_1512delinsCT	ENSP00000509861.1:p.Asp504Ala
ENST00000371953.8:c.992_993delinsCT MANE Select	ENSP00000361021.3:p.Asp331Ala
ENST00000371953.7:c.992_993delinsCT	ENSP00000361021.3:p.Asp331Ala
ENST00000472832.2:c.419_420delinsCT	ENSP00000483066.1:p.Asp140Ala
NM_000314.5:c.992_993delinsCT	NP_000305.3:p.Asp331Ala
NM_000314.6:c.992_993delinsCT	NP_000305.3:p.Asp331Ala
NM_001304717.2:c.1511_1512delinsCT	NP_001291646.2:p.Asp504Ala
NM_001304718.1:c.401_402delinsCT	NP_001291647.1:p.Asp134Ala
XM_006717926.2:c.947_948delinsCT	XP_006717989.1:p.Asp316Ala
XM_011539981.1:c.992_993delinsCT	XP_011538283.1:p.Asp331Ala
XM_011539982.1:c.896_897delinsCT	XP_011538284.1:p.Asp299Ala
XR_945791.1:n.1562_1563delinsCT
NM_000314.7:c.992_993delinsCT	NP_000305.3:p.Asp331Ala
NM_001304717.5:c.1511_1512delinsCT	NP_001291646.4:p.Asp504Ala
NM_001304718.2:c.401_402delinsCT	NP_001291647.1:p.Asp134Ala
NM_000314.8:c.992_993delinsCT MANE Select	NP_000305.3:p.Asp331Ala