Canonical Allele Identifier: CA891834847

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87960936_87960938delinsTAT , CM000672.2:g.87960936_87960938delinsTAT	GRCh38
NC_000010.10:g.89720693_89720695delinsTAT , CM000672.1:g.89720693_89720695delinsTAT	GRCh37
NC_000010.9:g.89710673_89710675delinsTAT	NCBI36
NG_007466.2:g.102498_102500delinsTAT , LRG_311:g.102498_102500delinsTAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.937_939delinsTAT	ENSP00000514759.2:p.Gly313Tyr
ENST00000710265.1:c.844_846delinsTAT	ENSP00000518161.1:p.Gly282Tyr
ENST00000472832.3:c.844_846delinsTAT	ENSP00000483066.2:p.Gly282Tyr
ENST00000688158.2:n.1579_1581delinsTAT
ENST00000688922.2:c.*674_*676delinsTAT	ENSP00000508742.2:n.*674_*676delinsTAT
ENST00000700021.1:c.799_801delinsTAT	ENSP00000514757.1:p.Gly267Tyr
ENST00000700022.1:c.*183_*185delinsTAT	ENSP00000514758.1:n.*183_*185delinsTAT
ENST00000700023.1:n.2002_2004delinsTAT
ENST00000700024.1:n.2236_2238delinsTAT
ENST00000700025.1:n.1613_1615delinsTAT
ENST00000700026.1:n.481_483delinsTAT
ENST00000700029.1:c.771_773delinsTAT
ENST00000706954.1:c.844_846delinsTAT	ENSP00000516674.1:p.Gly282Tyr
ENST00000706955.1:c.*879_*881delinsTAT	ENSP00000516675.1:n.*879_*881delinsTAT
ENST00000686459.1:c.*430_*432delinsTAT	ENSP00000508909.1:n.*430_*432delinsTAT
ENST00000688158.1:c.*955_*957delinsTAT	ENSP00000509254.1:n.*955_*957delinsTAT
ENST00000688308.1:c.844_846delinsTAT	ENSP00000508752.1:p.Gly282Tyr
ENST00000688922.1:c.765_767delinsTAT
ENST00000693560.1:c.1363_1365delinsTAT	ENSP00000509861.1:p.Gly455Tyr
ENST00000371953.8:c.844_846delinsTAT MANE Select	ENSP00000361021.3:p.Gly282Tyr
ENST00000371953.7:c.844_846delinsTAT	ENSP00000361021.3:p.Gly282Tyr
ENST00000472832.2:c.271_273delinsTAT	ENSP00000483066.1:p.Gly91Tyr
NM_000314.5:c.844_846delinsTAT	NP_000305.3:p.Gly282Tyr
NM_000314.6:c.844_846delinsTAT	NP_000305.3:p.Gly282Tyr
NM_001304717.2:c.1363_1365delinsTAT	NP_001291646.2:p.Gly455Tyr
NM_001304718.1:c.253_255delinsTAT	NP_001291647.1:p.Gly85Tyr
XM_006717926.2:c.799_801delinsTAT	XP_006717989.1:p.Gly267Tyr
XM_011539981.1:c.844_846delinsTAT	XP_011538283.1:p.Gly282Tyr
XM_011539982.1:c.748_750delinsTAT	XP_011538284.1:p.Gly250Tyr
XR_945791.1:n.1414_1416delinsTAT
NM_000314.7:c.844_846delinsTAT	NP_000305.3:p.Gly282Tyr
NM_001304717.5:c.1363_1365delinsTAT	NP_001291646.4:p.Gly455Tyr
NM_001304718.2:c.253_255delinsTAT	NP_001291647.1:p.Gly85Tyr
NM_000314.8:c.844_846delinsTAT MANE Select	NP_000305.3:p.Gly282Tyr