Canonical Allele Identifier: CA891840238

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87960912_87960914delinsCAT , CM000672.2:g.87960912_87960914delinsCAT	GRCh38
NC_000010.10:g.89720669_89720671delinsCAT , CM000672.1:g.89720669_89720671delinsCAT	GRCh37
NC_000010.9:g.89710649_89710651delinsCAT	NCBI36
NG_007466.2:g.102474_102476delinsCAT , LRG_311:g.102474_102476delinsCAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.913_915delinsCAT	ENSP00000514759.2:p.Trp305His
ENST00000710265.1:c.820_822delinsCAT	ENSP00000518161.1:p.Trp274His
ENST00000472832.3:c.820_822delinsCAT	ENSP00000483066.2:p.Trp274His
ENST00000688158.2:n.1555_1557delinsCAT
ENST00000688922.2:c.*650_*652delinsCAT	ENSP00000508742.2:n.*650_*652delinsCAT
ENST00000700021.1:c.775_777delinsCAT	ENSP00000514757.1:p.Trp259His
ENST00000700022.1:c.*159_*161delinsCAT	ENSP00000514758.1:n.*159_*161delinsCAT
ENST00000700023.1:n.1978_1980delinsCAT
ENST00000700024.1:n.2212_2214delinsCAT
ENST00000700025.1:n.1589_1591delinsCAT
ENST00000700026.1:n.457_459delinsCAT
ENST00000700029.1:c.747_749delinsCAT
ENST00000706954.1:c.820_822delinsCAT	ENSP00000516674.1:p.Trp274His
ENST00000706955.1:c.*855_*857delinsCAT	ENSP00000516675.1:n.*855_*857delinsCAT
ENST00000686459.1:c.*406_*408delinsCAT	ENSP00000508909.1:n.*406_*408delinsCAT
ENST00000688158.1:c.*931_*933delinsCAT	ENSP00000509254.1:n.*931_*933delinsCAT
ENST00000688308.1:c.820_822delinsCAT	ENSP00000508752.1:p.Trp274His
ENST00000688922.1:c.741_743delinsCAT
ENST00000693560.1:c.1339_1341delinsCAT	ENSP00000509861.1:p.Trp447His
ENST00000371953.8:c.820_822delinsCAT MANE Select	ENSP00000361021.3:p.Trp274His
ENST00000371953.7:c.820_822delinsCAT	ENSP00000361021.3:p.Trp274His
ENST00000472832.2:c.247_249delinsCAT	ENSP00000483066.1:p.Trp83His
NM_000314.5:c.820_822delinsCAT	NP_000305.3:p.Trp274His
NM_000314.6:c.820_822delinsCAT	NP_000305.3:p.Trp274His
NM_001304717.2:c.1339_1341delinsCAT	NP_001291646.2:p.Trp447His
NM_001304718.1:c.229_231delinsCAT	NP_001291647.1:p.Trp77His
XM_006717926.2:c.775_777delinsCAT	XP_006717989.1:p.Trp259His
XM_011539981.1:c.820_822delinsCAT	XP_011538283.1:p.Trp274His
XM_011539982.1:c.724_726delinsCAT	XP_011538284.1:p.Trp242His
XR_945791.1:n.1390_1392delinsCAT
NM_000314.7:c.820_822delinsCAT	NP_000305.3:p.Trp274His
NM_001304717.5:c.1339_1341delinsCAT	NP_001291646.4:p.Trp447His
NM_001304718.2:c.229_231delinsCAT	NP_001291647.1:p.Trp77His
NM_000314.8:c.820_822delinsCAT MANE Select	NP_000305.3:p.Trp274His