Canonical Allele Identifier: CA891835083

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87894072_87894074delinsTGT , CM000672.2:g.87894072_87894074delinsTGT	GRCh38
NC_000010.10:g.89653829_89653831delinsTGT , CM000672.1:g.89653829_89653831delinsTGT	GRCh37
NC_000010.9:g.89643809_89643811delinsTGT	NCBI36
NG_007466.2:g.35634_35636delinsTGT , LRG_311:g.35634_35636delinsTGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.127_129delinsTGT	ENSP00000514759.2:p.Glu43Cys
ENST00000710265.1:c.127_129delinsTGT	ENSP00000518161.1:p.Glu43Cys
ENST00000472832.3:c.127_129delinsTGT	ENSP00000483066.2:p.Glu43Cys
ENST00000688158.2:n.899+13634_899+13636delinsTGT
ENST00000688922.2:c.127_129delinsTGT	ENSP00000508742.2:p.Glu43Cys
ENST00000700021.1:c.127_129delinsTGT	ENSP00000514757.1:p.Glu43Cys
ENST00000700022.1:c.127_129delinsTGT	ENSP00000514758.1:p.Glu43Cys
ENST00000706954.1:c.127_129delinsTGT	ENSP00000516674.1:p.Glu43Cys
ENST00000706955.1:c.*162_*164delinsTGT	ENSP00000516675.1:n.*162_*164delinsTGT
ENST00000686459.1:c.127_129delinsTGT	ENSP00000508909.1:p.Glu43Cys
ENST00000688158.1:c.*275+13634_*275+13636delinsTGT	ENSP00000509254.1:n.*275+13634_*275+13636delinsTGT
ENST00000688308.1:c.127_129delinsTGT	ENSP00000508752.1:p.Glu43Cys
ENST00000693560.1:c.646_648delinsTGT	ENSP00000509861.1:p.Glu216Cys
ENST00000371953.8:c.127_129delinsTGT MANE Select	ENSP00000361021.3:p.Glu43Cys
ENST00000371953.7:c.127_129delinsTGT	ENSP00000361021.3:p.Glu43Cys
ENST00000462694.1:n.129_131delinsTGT
ENST00000610634.1:c.25_27delinsTGT	ENSP00000477517.1:p.Glu9Cys
NM_000314.5:c.127_129delinsTGT	NP_000305.3:p.Glu43Cys
NM_000314.6:c.127_129delinsTGT	NP_000305.3:p.Glu43Cys
NM_001304717.2:c.646_648delinsTGT	NP_001291646.2:p.Glu216Cys
NM_001304718.1:c.-579_-577delinsTGT	NP_001291647.1:n.-579_-577delinsTGT
XM_006717926.2:c.127_129delinsTGT	XP_006717989.1:p.Glu43Cys
XM_011539981.1:c.127_129delinsTGT	XP_011538283.1:p.Glu43Cys
XM_011539982.1:c.68+13634_68+13636delinsTGT	XP_011538284.1:n.68+13634_68+13636delinsTGT
XR_945789.1:n.839_841delinsTGT
XR_945790.1:n.839_841delinsTGT
XR_945791.1:n.839_841delinsTGT
NM_000314.7:c.127_129delinsTGT	NP_000305.3:p.Glu43Cys
NM_001304717.5:c.646_648delinsTGT	NP_001291646.4:p.Glu216Cys
NM_001304718.2:c.-579_-577delinsTGT	NP_001291647.1:n.-579_-577delinsTGT
NM_000314.8:c.127_129delinsTGT MANE Select	NP_000305.3:p.Glu43Cys