Canonical Allele Identifier: CA891841599

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87965356_87965357delinsGG , CM000672.2:g.87965356_87965357delinsGG	GRCh38
NC_000010.10:g.89725113_89725114delinsGG , CM000672.1:g.89725113_89725114delinsGG	GRCh37
NC_000010.9:g.89715093_89715094delinsGG	NCBI36
NG_007466.2:g.106918_106919delinsGG , LRG_311:g.106918_106919delinsGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.1189_1190delinsGG	ENSP00000514759.2:p.Thr397Gly
ENST00000710265.1:c.*125_*126delinsGG	ENSP00000518161.1:n.*125_*126delinsGG
ENST00000688158.2:n.1831_1832delinsGG
ENST00000688922.2:c.*926_*927delinsGG	ENSP00000508742.2:n.*926_*927delinsGG
ENST00000700021.1:c.1051_1052delinsGG	ENSP00000514757.1:p.Thr351Gly
ENST00000700022.1:c.*435_*436delinsGG	ENSP00000514758.1:n.*435_*436delinsGG
ENST00000700023.1:n.2254_2255delinsGG
ENST00000700024.1:n.2488_2489delinsGG
ENST00000706954.1:c.1096_1097delinsGG	ENSP00000516674.1:p.Thr366Gly
ENST00000706955.1:c.*1131_*1132delinsGG	ENSP00000516675.1:n.*1131_*1132delinsGG
ENST00000686459.1:c.*682_*683delinsGG	ENSP00000508909.1:n.*682_*683delinsGG
ENST00000688158.1:c.*1207_*1208delinsGG	ENSP00000509254.1:n.*1207_*1208delinsGG
ENST00000688308.1:c.1096_1097delinsGG	ENSP00000508752.1:p.Thr366Gly
ENST00000688922.1:c.1017_1018delinsGG
ENST00000693560.1:c.1615_1616delinsGG	ENSP00000509861.1:p.Thr539Gly
ENST00000371953.8:c.1096_1097delinsGG MANE Select	ENSP00000361021.3:p.Thr366Gly
ENST00000371953.7:c.1096_1097delinsGG	ENSP00000361021.3:p.Thr366Gly
NM_000314.5:c.1096_1097delinsGG	NP_000305.3:p.Thr366Gly
NM_000314.6:c.1096_1097delinsGG	NP_000305.3:p.Thr366Gly
NM_001304717.2:c.1615_1616delinsGG	NP_001291646.2:p.Thr539Gly
NM_001304718.1:c.505_506delinsGG	NP_001291647.1:p.Thr169Gly
XM_006717926.2:c.1051_1052delinsGG	XP_006717989.1:p.Thr351Gly
XM_011539982.1:c.1000_1001delinsGG	XP_011538284.1:p.Thr334Gly
XR_945791.1:n.1666_1667delinsGG
NM_000314.7:c.1096_1097delinsGG	NP_000305.3:p.Thr366Gly
NM_001304717.5:c.1615_1616delinsGG	NP_001291646.4:p.Thr539Gly
NM_001304718.2:c.505_506delinsGG	NP_001291647.1:p.Thr169Gly
NM_000314.8:c.1096_1097delinsGG MANE Select	NP_000305.3:p.Thr366Gly