Canonical Allele Identifier: CA891840963

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87958011_87958012delinsAC , CM000672.2:g.87958011_87958012delinsAC	GRCh38
NC_000010.10:g.89717768_89717769delinsAC , CM000672.1:g.89717768_89717769delinsAC	GRCh37
NC_000010.9:g.89707748_89707749delinsAC	NCBI36
NG_007466.2:g.99573_99574delinsAC , LRG_311:g.99573_99574delinsAC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.793_794delinsAC	ENSP00000514759.2:p.Leu265Thr
ENST00000710265.1:c.793_794delinsAC	ENSP00000518161.1:p.Leu265Thr
ENST00000472832.3:c.793_794delinsAC	ENSP00000483066.2:p.Leu265Thr
ENST00000688158.2:n.1528_1529delinsAC
ENST00000688922.2:c.*623_*624delinsAC	ENSP00000508742.2:n.*623_*624delinsAC
ENST00000700021.1:c.748_749delinsAC	ENSP00000514757.1:p.Leu250Thr
ENST00000700022.1:c.*132_*133delinsAC	ENSP00000514758.1:n.*132_*133delinsAC
ENST00000700023.1:n.1951_1952delinsAC
ENST00000700024.1:n.2185_2186delinsAC
ENST00000700025.1:n.1562_1563delinsAC
ENST00000700026.1:n.430_431delinsAC
ENST00000700029.1:c.627_628delinsAC
ENST00000706954.1:c.793_794delinsAC	ENSP00000516674.1:p.Leu265Thr
ENST00000706955.1:c.*828_*829delinsAC	ENSP00000516675.1:n.*828_*829delinsAC
ENST00000686459.1:c.*379_*380delinsAC	ENSP00000508909.1:n.*379_*380delinsAC
ENST00000688158.1:c.*904_*905delinsAC	ENSP00000509254.1:n.*904_*905delinsAC
ENST00000688308.1:c.793_794delinsAC	ENSP00000508752.1:p.Leu265Thr
ENST00000688922.1:c.714_715delinsAC
ENST00000693560.1:c.1312_1313delinsAC	ENSP00000509861.1:p.Leu438Thr
ENST00000371953.8:c.793_794delinsAC MANE Select	ENSP00000361021.3:p.Leu265Thr
ENST00000371953.7:c.793_794delinsAC	ENSP00000361021.3:p.Leu265Thr
ENST00000472832.2:c.220_221delinsAC	ENSP00000483066.1:p.Leu74Thr
NM_000314.5:c.793_794delinsAC	NP_000305.3:p.Leu265Thr
NM_000314.6:c.793_794delinsAC	NP_000305.3:p.Leu265Thr
NM_001304717.2:c.1312_1313delinsAC	NP_001291646.2:p.Leu438Thr
NM_001304718.1:c.202_203delinsAC	NP_001291647.1:p.Leu68Thr
XM_006717926.2:c.748_749delinsAC	XP_006717989.1:p.Leu250Thr
XM_011539981.1:c.793_794delinsAC	XP_011538283.1:p.Leu265Thr
XM_011539982.1:c.697_698delinsAC	XP_011538284.1:p.Leu233Thr
XR_945791.1:n.1363_1364delinsAC
NM_000314.7:c.793_794delinsAC	NP_000305.3:p.Leu265Thr
NM_001304717.5:c.1312_1313delinsAC	NP_001291646.4:p.Leu438Thr
NM_001304718.2:c.202_203delinsAC	NP_001291647.1:p.Leu68Thr
NM_000314.8:c.793_794delinsAC MANE Select	NP_000305.3:p.Leu265Thr