Canonical Allele Identifier: CA891840262

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87960918_87960919delinsTT , CM000672.2:g.87960918_87960919delinsTT	GRCh38
NC_000010.10:g.89720675_89720676delinsTT , CM000672.1:g.89720675_89720676delinsTT	GRCh37
NC_000010.9:g.89710655_89710656delinsTT	NCBI36
NG_007466.2:g.102480_102481delinsTT , LRG_311:g.102480_102481delinsTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.919_920delinsTT	ENSP00000514759.2:p.Asn307Phe
ENST00000710265.1:c.826_827delinsTT	ENSP00000518161.1:p.Asn276Phe
ENST00000472832.3:c.826_827delinsTT	ENSP00000483066.2:p.Asn276Phe
ENST00000688158.2:n.1561_1562delinsTT
ENST00000688922.2:c.*656_*657delinsTT	ENSP00000508742.2:n.*656_*657delinsTT
ENST00000700021.1:c.781_782delinsTT	ENSP00000514757.1:p.Asn261Phe
ENST00000700022.1:c.*165_*166delinsTT	ENSP00000514758.1:n.*165_*166delinsTT
ENST00000700023.1:n.1984_1985delinsTT
ENST00000700024.1:n.2218_2219delinsTT
ENST00000700025.1:n.1595_1596delinsTT
ENST00000700026.1:n.463_464delinsTT
ENST00000700029.1:c.753_754delinsTT
ENST00000706954.1:c.826_827delinsTT	ENSP00000516674.1:p.Asn276Phe
ENST00000706955.1:c.*861_*862delinsTT	ENSP00000516675.1:n.*861_*862delinsTT
ENST00000686459.1:c.*412_*413delinsTT	ENSP00000508909.1:n.*412_*413delinsTT
ENST00000688158.1:c.*937_*938delinsTT	ENSP00000509254.1:n.*937_*938delinsTT
ENST00000688308.1:c.826_827delinsTT	ENSP00000508752.1:p.Asn276Phe
ENST00000688922.1:c.747_748delinsTT
ENST00000693560.1:c.1345_1346delinsTT	ENSP00000509861.1:p.Asn449Phe
ENST00000371953.8:c.826_827delinsTT MANE Select	ENSP00000361021.3:p.Asn276Phe
ENST00000371953.7:c.826_827delinsTT	ENSP00000361021.3:p.Asn276Phe
ENST00000472832.2:c.253_254delinsTT	ENSP00000483066.1:p.Asn85Phe
NM_000314.5:c.826_827delinsTT	NP_000305.3:p.Asn276Phe
NM_000314.6:c.826_827delinsTT	NP_000305.3:p.Asn276Phe
NM_001304717.2:c.1345_1346delinsTT	NP_001291646.2:p.Asn449Phe
NM_001304718.1:c.235_236delinsTT	NP_001291647.1:p.Asn79Phe
XM_006717926.2:c.781_782delinsTT	XP_006717989.1:p.Asn261Phe
XM_011539981.1:c.826_827delinsTT	XP_011538283.1:p.Asn276Phe
XM_011539982.1:c.730_731delinsTT	XP_011538284.1:p.Asn244Phe
XR_945791.1:n.1396_1397delinsTT
NM_000314.7:c.826_827delinsTT	NP_000305.3:p.Asn276Phe
NM_001304717.5:c.1345_1346delinsTT	NP_001291646.4:p.Asn449Phe
NM_001304718.2:c.235_236delinsTT	NP_001291647.1:p.Asn79Phe
NM_000314.8:c.826_827delinsTT MANE Select	NP_000305.3:p.Asn276Phe