Canonical Allele Identifier: CA658822951

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87933063_87933067dup , CM000672.2:g.87933063_87933067dup	GRCh38
NC_000010.10:g.89692820_89692824dup , CM000672.1:g.89692820_89692824dup	GRCh37
NC_000010.9:g.89682800_89682804dup	NCBI36
NG_007466.2:g.74625_74629dup , LRG_311:g.74625_74629dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.304_308dup	ENSP00000514759.2:p.Phe104AsnfsTer11
ENST00000710265.1:c.304_308dup	ENSP00000518161.1:p.Phe104AsnfsTer11
ENST00000472832.3:c.304_308dup	ENSP00000483066.2:p.Phe104AsnfsTer11
ENST00000688158.2:n.1039_1043dup
ENST00000688922.2:c.*134_*138dup	ENSP00000508742.2:n.*134_*138dup
ENST00000700021.1:c.259_263dup	ENSP00000514757.1:p.Phe89AsnfsTer11
ENST00000700022.1:c.304_308dup	ENSP00000514758.1:p.Phe104AsnfsTer11
ENST00000700029.1:c.138_142dup
ENST00000706954.1:c.304_308dup	ENSP00000516674.1:p.Phe104AsnfsTer11
ENST00000706955.1:c.*339_*343dup	ENSP00000516675.1:n.*339_*343dup
ENST00000686459.1:c.304_308dup	ENSP00000508909.1:p.Phe104AsnfsTer11
ENST00000688158.1:c.*415_*419dup	ENSP00000509254.1:n.*415_*419dup
ENST00000688308.1:c.304_308dup	ENSP00000508752.1:p.Phe104AsnfsTer11
ENST00000688922.1:c.225_229dup
ENST00000693560.1:c.823_827dup	ENSP00000509861.1:p.Phe277AsnfsTer11
ENST00000371953.8:c.304_308dup MANE Select	ENSP00000361021.3:p.Phe104AsnfsTer11
ENST00000371953.7:c.304_308dup	ENSP00000361021.3:p.Phe104AsnfsTer11
ENST00000498703.1:n.130_134dup
ENST00000610634.1:c.202_206dup	ENSP00000477517.1:p.Phe70AsnfsTer11
NM_000314.5:c.304_308dup	NP_000305.3:p.Phe104AsnfsTer11
NM_000314.6:c.304_308dup	NP_000305.3:p.Phe104AsnfsTer11
NM_001304717.2:c.823_827dup	NP_001291646.2:p.Phe277AsnfsTer11
NM_001304718.1:c.-447_-443dup	NP_001291647.1:n.-447_-443dup
XM_006717926.2:c.259_263dup	XP_006717989.1:p.Phe89AsnfsTer11
XM_011539981.1:c.304_308dup	XP_011538283.1:p.Phe104AsnfsTer11
XM_011539982.1:c.208_212dup	XP_011538284.1:p.Phe72AsnfsTer11
XR_945789.1:n.1016_1020dup
XR_945790.1:n.1016_1020dup
XR_945791.1:n.1016_1020dup
NM_000314.7:c.304_308dup	NP_000305.3:p.Phe104AsnfsTer11
NM_001304717.5:c.823_827dup	NP_001291646.4:p.Phe277AsnfsTer11
NM_001304718.2:c.-447_-443dup	NP_001291647.1:n.-447_-443dup
NM_000314.8:c.304_308dup MANE Select	NP_000305.3:p.Phe104AsnfsTer11