Canonical Allele Identifier: CA891838463

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87933229_87933230delinsCT , CM000672.2:g.87933229_87933230delinsCT	GRCh38
NC_000010.10:g.89692986_89692987delinsCT , CM000672.1:g.89692986_89692987delinsCT	GRCh37
NC_000010.9:g.89682966_89682967delinsCT	NCBI36
NG_007466.2:g.74791_74792delinsCT , LRG_311:g.74791_74792delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.470_471delinsCT	ENSP00000514759.2:p.Glu157Ala
ENST00000710265.1:c.470_471delinsCT	ENSP00000518161.1:p.Glu157Ala
ENST00000472832.3:c.470_471delinsCT	ENSP00000483066.2:p.Glu157Ala
ENST00000688158.2:n.1205_1206delinsCT
ENST00000688922.2:c.*300_*301delinsCT	ENSP00000508742.2:n.*300_*301delinsCT
ENST00000700021.1:c.425_426delinsCT	ENSP00000514757.1:p.Glu142Ala
ENST00000700022.1:c.470_471delinsCT	ENSP00000514758.1:p.Glu157Ala
ENST00000700029.1:c.304_305delinsCT
ENST00000706954.1:c.470_471delinsCT	ENSP00000516674.1:p.Glu157Ala
ENST00000706955.1:c.*505_*506delinsCT	ENSP00000516675.1:n.*505_*506delinsCT
ENST00000686459.1:c.470_471delinsCT	ENSP00000508909.1:p.Glu157Ala
ENST00000688158.1:c.*581_*582delinsCT	ENSP00000509254.1:n.*581_*582delinsCT
ENST00000688308.1:c.470_471delinsCT	ENSP00000508752.1:p.Glu157Ala
ENST00000688922.1:c.391_392delinsCT
ENST00000693560.1:c.989_990delinsCT	ENSP00000509861.1:p.Glu330Ala
ENST00000371953.8:c.470_471delinsCT MANE Select	ENSP00000361021.3:p.Glu157Ala
ENST00000371953.7:c.470_471delinsCT	ENSP00000361021.3:p.Glu157Ala
ENST00000498703.1:n.296_297delinsCT
ENST00000610634.1:c.368_369delinsCT	ENSP00000477517.1:p.Glu123Ala
NM_000314.5:c.470_471delinsCT	NP_000305.3:p.Glu157Ala
NM_000314.6:c.470_471delinsCT	NP_000305.3:p.Glu157Ala
NM_001304717.2:c.989_990delinsCT	NP_001291646.2:p.Glu330Ala
NM_001304718.1:c.-281_-280delinsCT	NP_001291647.1:n.-281_-280delinsCT
XM_006717926.2:c.425_426delinsCT	XP_006717989.1:p.Glu142Ala
XM_011539981.1:c.470_471delinsCT	XP_011538283.1:p.Glu157Ala
XM_011539982.1:c.374_375delinsCT	XP_011538284.1:p.Glu125Ala
XR_945789.1:n.1182_1183delinsCT
XR_945790.1:n.1182_1183delinsCT
XR_945791.1:n.1182_1183delinsCT
NM_000314.7:c.470_471delinsCT	NP_000305.3:p.Glu157Ala
NM_001304717.5:c.989_990delinsCT	NP_001291646.4:p.Glu330Ala
NM_001304718.2:c.-281_-280delinsCT	NP_001291647.1:n.-281_-280delinsCT
NM_000314.8:c.470_471delinsCT MANE Select	NP_000305.3:p.Glu157Ala