Canonical Allele Identifier: CA891839407

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87957876_87957878delinsGGT , CM000672.2:g.87957876_87957878delinsGGT	GRCh38
NC_000010.10:g.89717633_89717635delinsGGT , CM000672.1:g.89717633_89717635delinsGGT	GRCh37
NC_000010.9:g.89707613_89707615delinsGGT	NCBI36
NG_007466.2:g.99438_99440delinsGGT , LRG_311:g.99438_99440delinsGGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.658_660delinsGGT	ENSP00000514759.2:p.Leu220Gly
ENST00000710265.1:c.658_660delinsGGT	ENSP00000518161.1:p.Leu220Gly
ENST00000472832.3:c.658_660delinsGGT	ENSP00000483066.2:p.Leu220Gly
ENST00000688158.2:n.1393_1395delinsGGT
ENST00000688922.2:c.*488_*490delinsGGT	ENSP00000508742.2:n.*488_*490delinsGGT
ENST00000700021.1:c.613_615delinsGGT	ENSP00000514757.1:p.Leu205Gly
ENST00000700022.1:c.516_518delinsGGT	ENSP00000514758.1:p.Ser172_Ter173delinsArgVal
ENST00000700023.1:n.1816_1818delinsGGT
ENST00000700024.1:n.2050_2052delinsGGT
ENST00000700025.1:n.1427_1429delinsGGT
ENST00000700026.1:n.295_297delinsGGT
ENST00000700029.1:c.492_494delinsGGT
ENST00000706954.1:c.658_660delinsGGT	ENSP00000516674.1:p.Leu220Gly
ENST00000706955.1:c.*693_*695delinsGGT	ENSP00000516675.1:n.*693_*695delinsGGT
ENST00000686459.1:c.*244_*246delinsGGT	ENSP00000508909.1:n.*244_*246delinsGGT
ENST00000688158.1:c.*769_*771delinsGGT	ENSP00000509254.1:n.*769_*771delinsGGT
ENST00000688308.1:c.658_660delinsGGT	ENSP00000508752.1:p.Leu220Gly
ENST00000688922.1:c.579_581delinsGGT
ENST00000693560.1:c.1177_1179delinsGGT	ENSP00000509861.1:p.Leu393Gly
ENST00000371953.8:c.658_660delinsGGT MANE Select	ENSP00000361021.3:p.Leu220Gly
ENST00000371953.7:c.658_660delinsGGT	ENSP00000361021.3:p.Leu220Gly
ENST00000472832.2:c.85_87delinsGGT	ENSP00000483066.1:p.Leu29Gly
NM_000314.5:c.658_660delinsGGT	NP_000305.3:p.Leu220Gly
NM_000314.6:c.658_660delinsGGT	NP_000305.3:p.Leu220Gly
NM_001304717.2:c.1177_1179delinsGGT	NP_001291646.2:p.Leu393Gly
NM_001304718.1:c.67_69delinsGGT	NP_001291647.1:p.Leu23Gly
XM_006717926.2:c.613_615delinsGGT	XP_006717989.1:p.Leu205Gly
XM_011539981.1:c.658_660delinsGGT	XP_011538283.1:p.Leu220Gly
XM_011539982.1:c.562_564delinsGGT	XP_011538284.1:p.Leu188Gly
XR_945791.1:n.1228_1230delinsGGT
NM_000314.7:c.658_660delinsGGT	NP_000305.3:p.Leu220Gly
NM_001304717.5:c.1177_1179delinsGGT	NP_001291646.4:p.Leu393Gly
NM_001304718.2:c.67_69delinsGGT	NP_001291647.1:p.Leu23Gly
NM_000314.8:c.658_660delinsGGT MANE Select	NP_000305.3:p.Leu220Gly