Canonical Allele Identifier: CA891834812

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87925524_87925525delinsGT , CM000672.2:g.87925524_87925525delinsGT	GRCh38
NC_000010.10:g.89685281_89685282delinsGT , CM000672.1:g.89685281_89685282delinsGT	GRCh37
NC_000010.9:g.89675261_89675262delinsGT	NCBI36
NG_007466.2:g.67086_67087delinsGT , LRG_311:g.67086_67087delinsGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.176_177delinsGT	ENSP00000514759.2:p.Ser59Cys
ENST00000710265.1:c.176_177delinsGT	ENSP00000518161.1:p.Ser59Cys
ENST00000472832.3:c.176_177delinsGT	ENSP00000483066.2:p.Ser59Cys
ENST00000688158.2:n.911_912delinsGT
ENST00000688922.2:c.176_177delinsGT	ENSP00000508742.2:p.Ser59Cys
ENST00000700021.1:c.165-5522_165-5521delinsGT	ENSP00000514757.1:n.165-5522_165-5521delinsGT
ENST00000700022.1:c.176_177delinsGT	ENSP00000514758.1:p.Ser59Cys
ENST00000700029.1:c.10_11delinsGT
ENST00000706954.1:c.176_177delinsGT	ENSP00000516674.1:p.Ser59Cys
ENST00000706955.1:c.*211_*212delinsGT	ENSP00000516675.1:n.*211_*212delinsGT
ENST00000686459.1:c.176_177delinsGT	ENSP00000508909.1:p.Ser59Cys
ENST00000688158.1:c.*287_*288delinsGT	ENSP00000509254.1:n.*287_*288delinsGT
ENST00000688308.1:c.176_177delinsGT	ENSP00000508752.1:p.Ser59Cys
ENST00000688922.1:c.45_46delinsGT
ENST00000693560.1:c.695_696delinsGT	ENSP00000509861.1:p.Ser232Cys
ENST00000371953.8:c.176_177delinsGT MANE Select	ENSP00000361021.3:p.Ser59Cys
ENST00000371953.7:c.176_177delinsGT	ENSP00000361021.3:p.Ser59Cys
ENST00000498703.1:n.2_3delinsGT
ENST00000610634.1:c.74_75delinsGT	ENSP00000477517.1:p.Ser25Cys
NM_000314.5:c.176_177delinsGT	NP_000305.3:p.Ser59Cys
NM_000314.6:c.176_177delinsGT	NP_000305.3:p.Ser59Cys
NM_001304717.2:c.695_696delinsGT	NP_001291646.2:p.Ser232Cys
NM_001304718.1:c.-541-5522_-541-5521delinsGT	NP_001291647.1:n.-541-5522_-541-5521delinsGT
XM_006717926.2:c.165-5522_165-5521delinsGT	XP_006717989.1:n.165-5522_165-5521delinsGT
XM_011539981.1:c.176_177delinsGT	XP_011538283.1:p.Ser59Cys
XM_011539982.1:c.80_81delinsGT	XP_011538284.1:p.Ser27Cys
XR_945789.1:n.888_889delinsGT
XR_945790.1:n.888_889delinsGT
XR_945791.1:n.888_889delinsGT
NM_000314.7:c.176_177delinsGT	NP_000305.3:p.Ser59Cys
NM_001304717.5:c.695_696delinsGT	NP_001291646.4:p.Ser232Cys
NM_001304718.2:c.-541-5522_-541-5521delinsGT	NP_001291647.1:n.-541-5522_-541-5521delinsGT
NM_000314.8:c.176_177delinsGT MANE Select	NP_000305.3:p.Ser59Cys