Canonical Allele Identifier: CA891837479

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87965356_87965357delinsCA , CM000672.2:g.87965356_87965357delinsCA	GRCh38
NC_000010.10:g.89725113_89725114delinsCA , CM000672.1:g.89725113_89725114delinsCA	GRCh37
NC_000010.9:g.89715093_89715094delinsCA	NCBI36
NG_007466.2:g.106918_106919delinsCA , LRG_311:g.106918_106919delinsCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.1189_1190delinsCA	ENSP00000514759.2:p.Thr397Gln
ENST00000710265.1:c.*125_*126delinsCA	ENSP00000518161.1:n.*125_*126delinsCA
ENST00000688158.2:n.1831_1832delinsCA
ENST00000688922.2:c.*926_*927delinsCA	ENSP00000508742.2:n.*926_*927delinsCA
ENST00000700021.1:c.1051_1052delinsCA	ENSP00000514757.1:p.Thr351Gln
ENST00000700022.1:c.*435_*436delinsCA	ENSP00000514758.1:n.*435_*436delinsCA
ENST00000700023.1:n.2254_2255delinsCA
ENST00000700024.1:n.2488_2489delinsCA
ENST00000706954.1:c.1096_1097delinsCA	ENSP00000516674.1:p.Thr366Gln
ENST00000706955.1:c.*1131_*1132delinsCA	ENSP00000516675.1:n.*1131_*1132delinsCA
ENST00000686459.1:c.*682_*683delinsCA	ENSP00000508909.1:n.*682_*683delinsCA
ENST00000688158.1:c.*1207_*1208delinsCA	ENSP00000509254.1:n.*1207_*1208delinsCA
ENST00000688308.1:c.1096_1097delinsCA	ENSP00000508752.1:p.Thr366Gln
ENST00000688922.1:c.1017_1018delinsCA
ENST00000693560.1:c.1615_1616delinsCA	ENSP00000509861.1:p.Thr539Gln
ENST00000371953.8:c.1096_1097delinsCA MANE Select	ENSP00000361021.3:p.Thr366Gln
ENST00000371953.7:c.1096_1097delinsCA	ENSP00000361021.3:p.Thr366Gln
NM_000314.5:c.1096_1097delinsCA	NP_000305.3:p.Thr366Gln
NM_000314.6:c.1096_1097delinsCA	NP_000305.3:p.Thr366Gln
NM_001304717.2:c.1615_1616delinsCA	NP_001291646.2:p.Thr539Gln
NM_001304718.1:c.505_506delinsCA	NP_001291647.1:p.Thr169Gln
XM_006717926.2:c.1051_1052delinsCA	XP_006717989.1:p.Thr351Gln
XM_011539982.1:c.1000_1001delinsCA	XP_011538284.1:p.Thr334Gln
XR_945791.1:n.1666_1667delinsCA
NM_000314.7:c.1096_1097delinsCA	NP_000305.3:p.Thr366Gln
NM_001304717.5:c.1615_1616delinsCA	NP_001291646.4:p.Thr539Gln
NM_001304718.2:c.505_506delinsCA	NP_001291647.1:p.Thr169Gln
NM_000314.8:c.1096_1097delinsCA MANE Select	NP_000305.3:p.Thr366Gln