Canonical Allele Identifier: CA2579927067

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87925523_87925525del , CM000672.2:g.87925523_87925525del	GRCh38
NC_000010.10:g.89685280_89685282del , CM000672.1:g.89685280_89685282del	GRCh37
NC_000010.9:g.89675260_89675262del	NCBI36
NG_007466.2:g.67085_67087del , LRG_311:g.67085_67087del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.175_177del	ENSP00000514759.2:p.Ser59del
ENST00000710265.1:c.175_177del	ENSP00000518161.1:p.Ser59del
ENST00000472832.3:c.175_177del	ENSP00000483066.2:p.Ser59del
ENST00000688158.2:n.910_912del
ENST00000688922.2:c.175_177del	ENSP00000508742.2:p.Ser59del
ENST00000700021.1:c.165-5523_165-5521del	ENSP00000514757.1:n.165-5523_165-5521del
ENST00000700022.1:c.175_177del	ENSP00000514758.1:p.Ser59del
ENST00000700029.1:c.9_11del
ENST00000706954.1:c.175_177del	ENSP00000516674.1:p.Ser59del
ENST00000706955.1:c.*210_*212del	ENSP00000516675.1:n.*210_*212del
ENST00000686459.1:c.175_177del	ENSP00000508909.1:p.Ser59del
ENST00000688158.1:c.*286_*288del	ENSP00000509254.1:n.*286_*288del
ENST00000688308.1:c.175_177del	ENSP00000508752.1:p.Ser59del
ENST00000688922.1:c.44_46del
ENST00000693560.1:c.694_696del	ENSP00000509861.1:p.Ser232del
ENST00000371953.8:c.175_177del MANE Select	ENSP00000361021.3:p.Ser59del
ENST00000371953.7:c.175_177del	ENSP00000361021.3:p.Ser59del
ENST00000498703.1:n.1_3del
ENST00000610634.1:c.73_75del	ENSP00000477517.1:p.Ser25del
NM_000314.5:c.175_177del	NP_000305.3:p.Ser59del
NM_000314.6:c.175_177del	NP_000305.3:p.Ser59del
NM_001304717.2:c.694_696del	NP_001291646.2:p.Ser232del
NM_001304718.1:c.-541-5523_-541-5521del	NP_001291647.1:n.-541-5523_-541-5521del
XM_006717926.2:c.165-5523_165-5521del	XP_006717989.1:n.165-5523_165-5521del
XM_011539981.1:c.175_177del	XP_011538283.1:p.Ser59del
XM_011539982.1:c.79_81del	XP_011538284.1:p.Ser27del
XR_945789.1:n.887_889del
XR_945790.1:n.887_889del
XR_945791.1:n.887_889del
NM_000314.7:c.175_177del	NP_000305.3:p.Ser59del
NM_001304717.5:c.694_696del	NP_001291646.4:p.Ser232del
NM_001304718.2:c.-541-5523_-541-5521del	NP_001291647.1:n.-541-5523_-541-5521del
NM_000314.8:c.175_177del MANE Select	NP_000305.3:p.Ser59del