Canonical Allele Identifier: CA891835369

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87894088_87894089delinsTT , CM000672.2:g.87894088_87894089delinsTT	GRCh38
NC_000010.10:g.89653845_89653846delinsTT , CM000672.1:g.89653845_89653846delinsTT	GRCh37
NC_000010.9:g.89643825_89643826delinsTT	NCBI36
NG_007466.2:g.35650_35651delinsTT , LRG_311:g.35650_35651delinsTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.143_144delinsTT	ENSP00000514759.2:p.Asn48Ile
ENST00000710265.1:c.143_144delinsTT	ENSP00000518161.1:p.Asn48Ile
ENST00000472832.3:c.143_144delinsTT	ENSP00000483066.2:p.Asn48Ile
ENST00000688158.2:n.899+13650_899+13651delinsTT
ENST00000688922.2:c.143_144delinsTT	ENSP00000508742.2:p.Asn48Ile
ENST00000700021.1:c.143_144delinsTT	ENSP00000514757.1:p.Asn48Ile
ENST00000700022.1:c.143_144delinsTT	ENSP00000514758.1:p.Asn48Ile
ENST00000706954.1:c.143_144delinsTT	ENSP00000516674.1:p.Asn48Ile
ENST00000706955.1:c.*178_*179delinsTT	ENSP00000516675.1:n.*178_*179delinsTT
ENST00000686459.1:c.143_144delinsTT	ENSP00000508909.1:p.Asn48Ile
ENST00000688158.1:c.*275+13650_*275+13651delinsTT	ENSP00000509254.1:n.*275+13650_*275+13651delinsTT
ENST00000688308.1:c.143_144delinsTT	ENSP00000508752.1:p.Asn48Ile
ENST00000688922.1:c.12_13delinsTT
ENST00000693560.1:c.662_663delinsTT	ENSP00000509861.1:p.Asn221Ile
ENST00000371953.8:c.143_144delinsTT MANE Select	ENSP00000361021.3:p.Asn48Ile
ENST00000371953.7:c.143_144delinsTT	ENSP00000361021.3:p.Asn48Ile
ENST00000462694.1:n.145_146delinsTT
ENST00000610634.1:c.41_42delinsTT	ENSP00000477517.1:p.Asn14Ile
NM_000314.5:c.143_144delinsTT	NP_000305.3:p.Asn48Ile
NM_000314.6:c.143_144delinsTT	NP_000305.3:p.Asn48Ile
NM_001304717.2:c.662_663delinsTT	NP_001291646.2:p.Asn221Ile
NM_001304718.1:c.-563_-562delinsTT	NP_001291647.1:n.-563_-562delinsTT
XM_006717926.2:c.143_144delinsTT	XP_006717989.1:p.Asn48Ile
XM_011539981.1:c.143_144delinsTT	XP_011538283.1:p.Asn48Ile
XM_011539982.1:c.68+13650_68+13651delinsTT	XP_011538284.1:n.68+13650_68+13651delinsTT
XR_945789.1:n.855_856delinsTT
XR_945790.1:n.855_856delinsTT
XR_945791.1:n.855_856delinsTT
NM_000314.7:c.143_144delinsTT	NP_000305.3:p.Asn48Ile
NM_001304717.5:c.662_663delinsTT	NP_001291646.4:p.Asn221Ile
NM_001304718.2:c.-563_-562delinsTT	NP_001291647.1:n.-563_-562delinsTT
NM_000314.8:c.143_144delinsTT MANE Select	NP_000305.3:p.Asn48Ile