Canonical Allele Identifier: CA891841150

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87960981_87960982delinsCC , CM000672.2:g.87960981_87960982delinsCC	GRCh38
NC_000010.10:g.89720738_89720739delinsCC , CM000672.1:g.89720738_89720739delinsCC	GRCh37
NC_000010.9:g.89710718_89710719delinsCC	NCBI36
NG_007466.2:g.102543_102544delinsCC , LRG_311:g.102543_102544delinsCC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.982_983delinsCC	ENSP00000514759.2:p.Asp328Pro
ENST00000710265.1:c.889_890delinsCC	ENSP00000518161.1:p.Asp297Pro
ENST00000472832.3:c.889_890delinsCC	ENSP00000483066.2:p.Asp297Pro
ENST00000688158.2:n.1624_1625delinsCC
ENST00000688922.2:c.*719_*720delinsCC	ENSP00000508742.2:n.*719_*720delinsCC
ENST00000700021.1:c.844_845delinsCC	ENSP00000514757.1:p.Asp282Pro
ENST00000700022.1:c.*228_*229delinsCC	ENSP00000514758.1:n.*228_*229delinsCC
ENST00000700023.1:n.2047_2048delinsCC
ENST00000700024.1:n.2281_2282delinsCC
ENST00000700025.1:n.1658_1659delinsCC
ENST00000700026.1:n.526_527delinsCC
ENST00000706954.1:c.889_890delinsCC	ENSP00000516674.1:p.Asp297Pro
ENST00000706955.1:c.*924_*925delinsCC	ENSP00000516675.1:n.*924_*925delinsCC
ENST00000686459.1:c.*475_*476delinsCC	ENSP00000508909.1:n.*475_*476delinsCC
ENST00000688158.1:c.*1000_*1001delinsCC	ENSP00000509254.1:n.*1000_*1001delinsCC
ENST00000688308.1:c.889_890delinsCC	ENSP00000508752.1:p.Asp297Pro
ENST00000688922.1:c.810_811delinsCC
ENST00000693560.1:c.1408_1409delinsCC	ENSP00000509861.1:p.Asp470Pro
ENST00000371953.8:c.889_890delinsCC MANE Select	ENSP00000361021.3:p.Asp297Pro
ENST00000371953.7:c.889_890delinsCC	ENSP00000361021.3:p.Asp297Pro
ENST00000472832.2:c.316_317delinsCC	ENSP00000483066.1:p.Asp106Pro
NM_000314.5:c.889_890delinsCC	NP_000305.3:p.Asp297Pro
NM_000314.6:c.889_890delinsCC	NP_000305.3:p.Asp297Pro
NM_001304717.2:c.1408_1409delinsCC	NP_001291646.2:p.Asp470Pro
NM_001304718.1:c.298_299delinsCC	NP_001291647.1:p.Asp100Pro
XM_006717926.2:c.844_845delinsCC	XP_006717989.1:p.Asp282Pro
XM_011539981.1:c.889_890delinsCC	XP_011538283.1:p.Asp297Pro
XM_011539982.1:c.793_794delinsCC	XP_011538284.1:p.Asp265Pro
XR_945791.1:n.1459_1460delinsCC
NM_000314.7:c.889_890delinsCC	NP_000305.3:p.Asp297Pro
NM_001304717.5:c.1408_1409delinsCC	NP_001291646.4:p.Asp470Pro
NM_001304718.2:c.298_299delinsCC	NP_001291647.1:p.Asp100Pro
NM_000314.8:c.889_890delinsCC MANE Select	NP_000305.3:p.Asp297Pro