Canonical Allele Identifier: CA891835508

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87960981_87960982delinsTT , CM000672.2:g.87960981_87960982delinsTT	GRCh38
NC_000010.10:g.89720738_89720739delinsTT , CM000672.1:g.89720738_89720739delinsTT	GRCh37
NC_000010.9:g.89710718_89710719delinsTT	NCBI36
NG_007466.2:g.102543_102544delinsTT , LRG_311:g.102543_102544delinsTT

Transcript Alleles

HGVS	Amino-acid change
ENST00000700029.2:c.982_983delinsTT	ENSP00000514759.2:p.Asp328Phe
ENST00000710265.1:c.889_890delinsTT	ENSP00000518161.1:p.Asp297Phe
ENST00000472832.3:c.889_890delinsTT	ENSP00000483066.2:p.Asp297Phe
ENST00000688158.2:n.1624_1625delinsTT
ENST00000688922.2:c.*719_*720delinsTT	ENSP00000508742.2:n.*719_*720delinsTT
ENST00000700021.1:c.844_845delinsTT	ENSP00000514757.1:p.Asp282Phe
ENST00000700022.1:c.*228_*229delinsTT	ENSP00000514758.1:n.*228_*229delinsTT
ENST00000700023.1:n.2047_2048delinsTT
ENST00000700024.1:n.2281_2282delinsTT
ENST00000700025.1:n.1658_1659delinsTT
ENST00000700026.1:n.526_527delinsTT
ENST00000706954.1:c.889_890delinsTT	ENSP00000516674.1:p.Asp297Phe
ENST00000706955.1:c.*924_*925delinsTT	ENSP00000516675.1:n.*924_*925delinsTT
ENST00000686459.1:c.*475_*476delinsTT	ENSP00000508909.1:n.*475_*476delinsTT
ENST00000688158.1:c.*1000_*1001delinsTT	ENSP00000509254.1:n.*1000_*1001delinsTT
ENST00000688308.1:c.889_890delinsTT	ENSP00000508752.1:p.Asp297Phe
ENST00000688922.1:c.810_811delinsTT
ENST00000693560.1:c.1408_1409delinsTT	ENSP00000509861.1:p.Asp470Phe
ENST00000371953.8:c.889_890delinsTT MANE Select	ENSP00000361021.3:p.Asp297Phe
ENST00000371953.7:c.889_890delinsTT	ENSP00000361021.3:p.Asp297Phe
ENST00000472832.2:c.316_317delinsTT	ENSP00000483066.1:p.Asp106Phe
NM_000314.5:c.889_890delinsTT	NP_000305.3:p.Asp297Phe
NM_000314.6:c.889_890delinsTT	NP_000305.3:p.Asp297Phe
NM_001304717.2:c.1408_1409delinsTT	NP_001291646.2:p.Asp470Phe
NM_001304718.1:c.298_299delinsTT	NP_001291647.1:p.Asp100Phe
XM_006717926.2:c.844_845delinsTT	XP_006717989.1:p.Asp282Phe
XM_011539981.1:c.889_890delinsTT	XP_011538283.1:p.Asp297Phe
XM_011539982.1:c.793_794delinsTT	XP_011538284.1:p.Asp265Phe
XR_945791.1:n.1459_1460delinsTT
NM_000314.7:c.889_890delinsTT	NP_000305.3:p.Asp297Phe
NM_001304717.5:c.1408_1409delinsTT	NP_001291646.4:p.Asp470Phe
NM_001304718.2:c.298_299delinsTT	NP_001291647.1:p.Asp100Phe
NM_000314.8:c.889_890delinsTT MANE Select	NP_000305.3:p.Asp297Phe