Canonical Allele Identifier: CA891840234

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87960912_87960914delinsGCT , CM000672.2:g.87960912_87960914delinsGCT	GRCh38
NC_000010.10:g.89720669_89720671delinsGCT , CM000672.1:g.89720669_89720671delinsGCT	GRCh37
NC_000010.9:g.89710649_89710651delinsGCT	NCBI36
NG_007466.2:g.102474_102476delinsGCT , LRG_311:g.102474_102476delinsGCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.913_915delinsGCT	ENSP00000514759.2:p.Trp305Ala
ENST00000710265.1:c.820_822delinsGCT	ENSP00000518161.1:p.Trp274Ala
ENST00000472832.3:c.820_822delinsGCT	ENSP00000483066.2:p.Trp274Ala
ENST00000688158.2:n.1555_1557delinsGCT
ENST00000688922.2:c.*650_*652delinsGCT	ENSP00000508742.2:n.*650_*652delinsGCT
ENST00000700021.1:c.775_777delinsGCT	ENSP00000514757.1:p.Trp259Ala
ENST00000700022.1:c.*159_*161delinsGCT	ENSP00000514758.1:n.*159_*161delinsGCT
ENST00000700023.1:n.1978_1980delinsGCT
ENST00000700024.1:n.2212_2214delinsGCT
ENST00000700025.1:n.1589_1591delinsGCT
ENST00000700026.1:n.457_459delinsGCT
ENST00000700029.1:c.747_749delinsGCT
ENST00000706954.1:c.820_822delinsGCT	ENSP00000516674.1:p.Trp274Ala
ENST00000706955.1:c.*855_*857delinsGCT	ENSP00000516675.1:n.*855_*857delinsGCT
ENST00000686459.1:c.*406_*408delinsGCT	ENSP00000508909.1:n.*406_*408delinsGCT
ENST00000688158.1:c.*931_*933delinsGCT	ENSP00000509254.1:n.*931_*933delinsGCT
ENST00000688308.1:c.820_822delinsGCT	ENSP00000508752.1:p.Trp274Ala
ENST00000688922.1:c.741_743delinsGCT
ENST00000693560.1:c.1339_1341delinsGCT	ENSP00000509861.1:p.Trp447Ala
ENST00000371953.8:c.820_822delinsGCT MANE Select	ENSP00000361021.3:p.Trp274Ala
ENST00000371953.7:c.820_822delinsGCT	ENSP00000361021.3:p.Trp274Ala
ENST00000472832.2:c.247_249delinsGCT	ENSP00000483066.1:p.Trp83Ala
NM_000314.5:c.820_822delinsGCT	NP_000305.3:p.Trp274Ala
NM_000314.6:c.820_822delinsGCT	NP_000305.3:p.Trp274Ala
NM_001304717.2:c.1339_1341delinsGCT	NP_001291646.2:p.Trp447Ala
NM_001304718.1:c.229_231delinsGCT	NP_001291647.1:p.Trp77Ala
XM_006717926.2:c.775_777delinsGCT	XP_006717989.1:p.Trp259Ala
XM_011539981.1:c.820_822delinsGCT	XP_011538283.1:p.Trp274Ala
XM_011539982.1:c.724_726delinsGCT	XP_011538284.1:p.Trp242Ala
XR_945791.1:n.1390_1392delinsGCT
NM_000314.7:c.820_822delinsGCT	NP_000305.3:p.Trp274Ala
NM_001304717.5:c.1339_1341delinsGCT	NP_001291646.4:p.Trp447Ala
NM_001304718.2:c.229_231delinsGCT	NP_001291647.1:p.Trp77Ala
NM_000314.8:c.820_822delinsGCT MANE Select	NP_000305.3:p.Trp274Ala