Canonical Allele Identifier: CA891836903

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87961084_87961085delinsTT , CM000672.2:g.87961084_87961085delinsTT	GRCh38
NC_000010.10:g.89720841_89720842delinsTT , CM000672.1:g.89720841_89720842delinsTT	GRCh37
NC_000010.9:g.89710821_89710822delinsTT	NCBI36
NG_007466.2:g.102646_102647delinsTT , LRG_311:g.102646_102647delinsTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.1085_1086delinsTT	ENSP00000514759.2:p.Asp362Val
ENST00000710265.1:c.992_993delinsTT	ENSP00000518161.1:p.Asp331Val
ENST00000472832.3:c.992_993delinsTT	ENSP00000483066.2:p.Asp331Val
ENST00000688158.2:n.1727_1728delinsTT
ENST00000688922.2:c.*822_*823delinsTT	ENSP00000508742.2:n.*822_*823delinsTT
ENST00000700021.1:c.947_948delinsTT	ENSP00000514757.1:p.Asp316Val
ENST00000700022.1:c.*331_*332delinsTT	ENSP00000514758.1:n.*331_*332delinsTT
ENST00000700023.1:n.2150_2151delinsTT
ENST00000700024.1:n.2384_2385delinsTT
ENST00000700025.1:n.1761_1762delinsTT
ENST00000700026.1:n.629_630delinsTT
ENST00000706954.1:c.992_993delinsTT	ENSP00000516674.1:p.Asp331Val
ENST00000706955.1:c.*1027_*1028delinsTT	ENSP00000516675.1:n.*1027_*1028delinsTT
ENST00000686459.1:c.*578_*579delinsTT	ENSP00000508909.1:n.*578_*579delinsTT
ENST00000688158.1:c.*1103_*1104delinsTT	ENSP00000509254.1:n.*1103_*1104delinsTT
ENST00000688308.1:c.992_993delinsTT	ENSP00000508752.1:p.Asp331Val
ENST00000688922.1:c.913_914delinsTT
ENST00000693560.1:c.1511_1512delinsTT	ENSP00000509861.1:p.Asp504Val
ENST00000371953.8:c.992_993delinsTT MANE Select	ENSP00000361021.3:p.Asp331Val
ENST00000371953.7:c.992_993delinsTT	ENSP00000361021.3:p.Asp331Val
ENST00000472832.2:c.419_420delinsTT	ENSP00000483066.1:p.Asp140Val
NM_000314.5:c.992_993delinsTT	NP_000305.3:p.Asp331Val
NM_000314.6:c.992_993delinsTT	NP_000305.3:p.Asp331Val
NM_001304717.2:c.1511_1512delinsTT	NP_001291646.2:p.Asp504Val
NM_001304718.1:c.401_402delinsTT	NP_001291647.1:p.Asp134Val
XM_006717926.2:c.947_948delinsTT	XP_006717989.1:p.Asp316Val
XM_011539981.1:c.992_993delinsTT	XP_011538283.1:p.Asp331Val
XM_011539982.1:c.896_897delinsTT	XP_011538284.1:p.Asp299Val
XR_945791.1:n.1562_1563delinsTT
NM_000314.7:c.992_993delinsTT	NP_000305.3:p.Asp331Val
NM_001304717.5:c.1511_1512delinsTT	NP_001291646.4:p.Asp504Val
NM_001304718.2:c.401_402delinsTT	NP_001291647.1:p.Asp134Val
NM_000314.8:c.992_993delinsTT MANE Select	NP_000305.3:p.Asp331Val