Canonical Allele Identifier: CA891837476

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87965356_87965358delinsGAT , CM000672.2:g.87965356_87965358delinsGAT	GRCh38
NC_000010.10:g.89725113_89725115delinsGAT , CM000672.1:g.89725113_89725115delinsGAT	GRCh37
NC_000010.9:g.89715093_89715095delinsGAT	NCBI36
NG_007466.2:g.106918_106920delinsGAT , LRG_311:g.106918_106920delinsGAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.1189_1191delinsGAT	ENSP00000514759.2:p.Thr397Asp
ENST00000710265.1:c.*125_*127delinsGAT	ENSP00000518161.1:n.*125_*127delinsGAT
ENST00000688158.2:n.1831_1833delinsGAT
ENST00000688922.2:c.*926_*928delinsGAT	ENSP00000508742.2:n.*926_*928delinsGAT
ENST00000700021.1:c.1051_1053delinsGAT	ENSP00000514757.1:p.Thr351Asp
ENST00000700022.1:c.*435_*437delinsGAT	ENSP00000514758.1:n.*435_*437delinsGAT
ENST00000700023.1:n.2254_2256delinsGAT
ENST00000700024.1:n.2488_2490delinsGAT
ENST00000706954.1:c.1096_1098delinsGAT	ENSP00000516674.1:p.Thr366Asp
ENST00000706955.1:c.*1131_*1133delinsGAT	ENSP00000516675.1:n.*1131_*1133delinsGAT
ENST00000686459.1:c.*682_*684delinsGAT	ENSP00000508909.1:n.*682_*684delinsGAT
ENST00000688158.1:c.*1207_*1209delinsGAT	ENSP00000509254.1:n.*1207_*1209delinsGAT
ENST00000688308.1:c.1096_1098delinsGAT	ENSP00000508752.1:p.Thr366Asp
ENST00000688922.1:c.1017_1019delinsGAT
ENST00000693560.1:c.1615_1617delinsGAT	ENSP00000509861.1:p.Thr539Asp
ENST00000371953.8:c.1096_1098delinsGAT MANE Select	ENSP00000361021.3:p.Thr366Asp
ENST00000371953.7:c.1096_1098delinsGAT	ENSP00000361021.3:p.Thr366Asp
NM_000314.5:c.1096_1098delinsGAT	NP_000305.3:p.Thr366Asp
NM_000314.6:c.1096_1098delinsGAT	NP_000305.3:p.Thr366Asp
NM_001304717.2:c.1615_1617delinsGAT	NP_001291646.2:p.Thr539Asp
NM_001304718.1:c.505_507delinsGAT	NP_001291647.1:p.Thr169Asp
XM_006717926.2:c.1051_1053delinsGAT	XP_006717989.1:p.Thr351Asp
XM_011539982.1:c.1000_1002delinsGAT	XP_011538284.1:p.Thr334Asp
XR_945791.1:n.1666_1668delinsGAT
NM_000314.7:c.1096_1098delinsGAT	NP_000305.3:p.Thr366Asp
NM_001304717.5:c.1615_1617delinsGAT	NP_001291646.4:p.Thr539Asp
NM_001304718.2:c.505_507delinsGAT	NP_001291647.1:p.Thr169Asp
NM_000314.8:c.1096_1098delinsGAT MANE Select	NP_000305.3:p.Thr366Asp