Canonical Allele Identifier: CA891835126

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87960954_87960956delinsTAT , CM000672.2:g.87960954_87960956delinsTAT	GRCh38
NC_000010.10:g.89720711_89720713delinsTAT , CM000672.1:g.89720711_89720713delinsTAT	GRCh37
NC_000010.9:g.89710691_89710693delinsTAT	NCBI36
NG_007466.2:g.102516_102518delinsTAT , LRG_311:g.102516_102518delinsTAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.955_957delinsTAT	ENSP00000514759.2:p.Glu319Tyr
ENST00000710265.1:c.862_864delinsTAT	ENSP00000518161.1:p.Glu288Tyr
ENST00000472832.3:c.862_864delinsTAT	ENSP00000483066.2:p.Glu288Tyr
ENST00000688158.2:n.1597_1599delinsTAT
ENST00000688922.2:c.*692_*694delinsTAT	ENSP00000508742.2:n.*692_*694delinsTAT
ENST00000700021.1:c.817_819delinsTAT	ENSP00000514757.1:p.Glu273Tyr
ENST00000700022.1:c.*201_*203delinsTAT	ENSP00000514758.1:n.*201_*203delinsTAT
ENST00000700023.1:n.2020_2022delinsTAT
ENST00000700024.1:n.2254_2256delinsTAT
ENST00000700025.1:n.1631_1633delinsTAT
ENST00000700026.1:n.499_501delinsTAT
ENST00000700029.1:c.789_791delinsTAT
ENST00000706954.1:c.862_864delinsTAT	ENSP00000516674.1:p.Glu288Tyr
ENST00000706955.1:c.*897_*899delinsTAT	ENSP00000516675.1:n.*897_*899delinsTAT
ENST00000686459.1:c.*448_*450delinsTAT	ENSP00000508909.1:n.*448_*450delinsTAT
ENST00000688158.1:c.*973_*975delinsTAT	ENSP00000509254.1:n.*973_*975delinsTAT
ENST00000688308.1:c.862_864delinsTAT	ENSP00000508752.1:p.Glu288Tyr
ENST00000688922.1:c.783_785delinsTAT
ENST00000693560.1:c.1381_1383delinsTAT	ENSP00000509861.1:p.Glu461Tyr
ENST00000371953.8:c.862_864delinsTAT MANE Select	ENSP00000361021.3:p.Glu288Tyr
ENST00000371953.7:c.862_864delinsTAT	ENSP00000361021.3:p.Glu288Tyr
ENST00000472832.2:c.289_291delinsTAT	ENSP00000483066.1:p.Glu97Tyr
NM_000314.5:c.862_864delinsTAT	NP_000305.3:p.Glu288Tyr
NM_000314.6:c.862_864delinsTAT	NP_000305.3:p.Glu288Tyr
NM_001304717.2:c.1381_1383delinsTAT	NP_001291646.2:p.Glu461Tyr
NM_001304718.1:c.271_273delinsTAT	NP_001291647.1:p.Glu91Tyr
XM_006717926.2:c.817_819delinsTAT	XP_006717989.1:p.Glu273Tyr
XM_011539981.1:c.862_864delinsTAT	XP_011538283.1:p.Glu288Tyr
XM_011539982.1:c.766_768delinsTAT	XP_011538284.1:p.Glu256Tyr
XR_945791.1:n.1432_1434delinsTAT
NM_000314.7:c.862_864delinsTAT	NP_000305.3:p.Glu288Tyr
NM_001304717.5:c.1381_1383delinsTAT	NP_001291646.4:p.Glu461Tyr
NM_001304718.2:c.271_273delinsTAT	NP_001291647.1:p.Glu91Tyr
NM_000314.8:c.862_864delinsTAT MANE Select	NP_000305.3:p.Glu288Tyr