Canonical Allele Identifier: CA891837109

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87965317_87965319delinsTCT , CM000672.2:g.87965317_87965319delinsTCT	GRCh38
NC_000010.10:g.89725074_89725076delinsTCT , CM000672.1:g.89725074_89725076delinsTCT	GRCh37
NC_000010.9:g.89715054_89715056delinsTCT	NCBI36
NG_007466.2:g.106879_106881delinsTCT , LRG_311:g.106879_106881delinsTCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.1150_1152delinsTCT	ENSP00000514759.2:p.Glu384Ser
ENST00000710265.1:c.*86_*88delinsTCT	ENSP00000518161.1:n.*86_*88delinsTCT
ENST00000688158.2:n.1792_1794delinsTCT
ENST00000688922.2:c.*887_*889delinsTCT	ENSP00000508742.2:n.*887_*889delinsTCT
ENST00000700021.1:c.1012_1014delinsTCT	ENSP00000514757.1:p.Glu338Ser
ENST00000700022.1:c.*396_*398delinsTCT	ENSP00000514758.1:n.*396_*398delinsTCT
ENST00000700023.1:n.2215_2217delinsTCT
ENST00000700024.1:n.2449_2451delinsTCT
ENST00000706954.1:c.1057_1059delinsTCT	ENSP00000516674.1:p.Glu353Ser
ENST00000706955.1:c.*1092_*1094delinsTCT	ENSP00000516675.1:n.*1092_*1094delinsTCT
ENST00000686459.1:c.*643_*645delinsTCT	ENSP00000508909.1:n.*643_*645delinsTCT
ENST00000688158.1:c.*1168_*1170delinsTCT	ENSP00000509254.1:n.*1168_*1170delinsTCT
ENST00000688308.1:c.1057_1059delinsTCT	ENSP00000508752.1:p.Glu353Ser
ENST00000688922.1:c.978_980delinsTCT
ENST00000693560.1:c.1576_1578delinsTCT	ENSP00000509861.1:p.Glu526Ser
ENST00000371953.8:c.1057_1059delinsTCT MANE Select	ENSP00000361021.3:p.Glu353Ser
ENST00000371953.7:c.1057_1059delinsTCT	ENSP00000361021.3:p.Glu353Ser
NM_000314.5:c.1057_1059delinsTCT	NP_000305.3:p.Glu353Ser
NM_000314.6:c.1057_1059delinsTCT	NP_000305.3:p.Glu353Ser
NM_001304717.2:c.1576_1578delinsTCT	NP_001291646.2:p.Glu526Ser
NM_001304718.1:c.466_468delinsTCT	NP_001291647.1:p.Glu156Ser
XM_006717926.2:c.1012_1014delinsTCT	XP_006717989.1:p.Glu338Ser
XM_011539982.1:c.961_963delinsTCT	XP_011538284.1:p.Glu321Ser
XR_945791.1:n.1627_1629delinsTCT
NM_000314.7:c.1057_1059delinsTCT	NP_000305.3:p.Glu353Ser
NM_001304717.5:c.1576_1578delinsTCT	NP_001291646.4:p.Glu526Ser
NM_001304718.2:c.466_468delinsTCT	NP_001291647.1:p.Glu156Ser
NM_000314.8:c.1057_1059delinsTCT MANE Select	NP_000305.3:p.Glu353Ser