Canonical Allele Identifier: CA891839410

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87957876_87957878delinsACT , CM000672.2:g.87957876_87957878delinsACT	GRCh38
NC_000010.10:g.89717633_89717635delinsACT , CM000672.1:g.89717633_89717635delinsACT	GRCh37
NC_000010.9:g.89707613_89707615delinsACT	NCBI36
NG_007466.2:g.99438_99440delinsACT , LRG_311:g.99438_99440delinsACT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.658_660delinsACT	ENSP00000514759.2:p.Leu220Thr
ENST00000710265.1:c.658_660delinsACT	ENSP00000518161.1:p.Leu220Thr
ENST00000472832.3:c.658_660delinsACT	ENSP00000483066.2:p.Leu220Thr
ENST00000688158.2:n.1393_1395delinsACT
ENST00000688922.2:c.*488_*490delinsACT	ENSP00000508742.2:n.*488_*490delinsACT
ENST00000700021.1:c.613_615delinsACT	ENSP00000514757.1:p.Leu205Thr
ENST00000700022.1:c.516_518delinsACT	ENSP00000514758.1:p.Ser172_Ter173delinsArgLeu
ENST00000700023.1:n.1816_1818delinsACT
ENST00000700024.1:n.2050_2052delinsACT
ENST00000700025.1:n.1427_1429delinsACT
ENST00000700026.1:n.295_297delinsACT
ENST00000700029.1:c.492_494delinsACT
ENST00000706954.1:c.658_660delinsACT	ENSP00000516674.1:p.Leu220Thr
ENST00000706955.1:c.*693_*695delinsACT	ENSP00000516675.1:n.*693_*695delinsACT
ENST00000686459.1:c.*244_*246delinsACT	ENSP00000508909.1:n.*244_*246delinsACT
ENST00000688158.1:c.*769_*771delinsACT	ENSP00000509254.1:n.*769_*771delinsACT
ENST00000688308.1:c.658_660delinsACT	ENSP00000508752.1:p.Leu220Thr
ENST00000688922.1:c.579_581delinsACT
ENST00000693560.1:c.1177_1179delinsACT	ENSP00000509861.1:p.Leu393Thr
ENST00000371953.8:c.658_660delinsACT MANE Select	ENSP00000361021.3:p.Leu220Thr
ENST00000371953.7:c.658_660delinsACT	ENSP00000361021.3:p.Leu220Thr
ENST00000472832.2:c.85_87delinsACT	ENSP00000483066.1:p.Leu29Thr
NM_000314.5:c.658_660delinsACT	NP_000305.3:p.Leu220Thr
NM_000314.6:c.658_660delinsACT	NP_000305.3:p.Leu220Thr
NM_001304717.2:c.1177_1179delinsACT	NP_001291646.2:p.Leu393Thr
NM_001304718.1:c.67_69delinsACT	NP_001291647.1:p.Leu23Thr
XM_006717926.2:c.613_615delinsACT	XP_006717989.1:p.Leu205Thr
XM_011539981.1:c.658_660delinsACT	XP_011538283.1:p.Leu220Thr
XM_011539982.1:c.562_564delinsACT	XP_011538284.1:p.Leu188Thr
XR_945791.1:n.1228_1230delinsACT
NM_000314.7:c.658_660delinsACT	NP_000305.3:p.Leu220Thr
NM_001304717.5:c.1177_1179delinsACT	NP_001291646.4:p.Leu393Thr
NM_001304718.2:c.67_69delinsACT	NP_001291647.1:p.Leu23Thr
NM_000314.8:c.658_660delinsACT MANE Select	NP_000305.3:p.Leu220Thr