Canonical Allele Identifier: CA891834832

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87960936_87960938delinsTCT , CM000672.2:g.87960936_87960938delinsTCT	GRCh38
NC_000010.10:g.89720693_89720695delinsTCT , CM000672.1:g.89720693_89720695delinsTCT	GRCh37
NC_000010.9:g.89710673_89710675delinsTCT	NCBI36
NG_007466.2:g.102498_102500delinsTCT , LRG_311:g.102498_102500delinsTCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.937_939delinsTCT	ENSP00000514759.2:p.Gly313Ser
ENST00000710265.1:c.844_846delinsTCT	ENSP00000518161.1:p.Gly282Ser
ENST00000472832.3:c.844_846delinsTCT	ENSP00000483066.2:p.Gly282Ser
ENST00000688158.2:n.1579_1581delinsTCT
ENST00000688922.2:c.*674_*676delinsTCT	ENSP00000508742.2:n.*674_*676delinsTCT
ENST00000700021.1:c.799_801delinsTCT	ENSP00000514757.1:p.Gly267Ser
ENST00000700022.1:c.*183_*185delinsTCT	ENSP00000514758.1:n.*183_*185delinsTCT
ENST00000700023.1:n.2002_2004delinsTCT
ENST00000700024.1:n.2236_2238delinsTCT
ENST00000700025.1:n.1613_1615delinsTCT
ENST00000700026.1:n.481_483delinsTCT
ENST00000700029.1:c.771_773delinsTCT
ENST00000706954.1:c.844_846delinsTCT	ENSP00000516674.1:p.Gly282Ser
ENST00000706955.1:c.*879_*881delinsTCT	ENSP00000516675.1:n.*879_*881delinsTCT
ENST00000686459.1:c.*430_*432delinsTCT	ENSP00000508909.1:n.*430_*432delinsTCT
ENST00000688158.1:c.*955_*957delinsTCT	ENSP00000509254.1:n.*955_*957delinsTCT
ENST00000688308.1:c.844_846delinsTCT	ENSP00000508752.1:p.Gly282Ser
ENST00000688922.1:c.765_767delinsTCT
ENST00000693560.1:c.1363_1365delinsTCT	ENSP00000509861.1:p.Gly455Ser
ENST00000371953.8:c.844_846delinsTCT MANE Select	ENSP00000361021.3:p.Gly282Ser
ENST00000371953.7:c.844_846delinsTCT	ENSP00000361021.3:p.Gly282Ser
ENST00000472832.2:c.271_273delinsTCT	ENSP00000483066.1:p.Gly91Ser
NM_000314.5:c.844_846delinsTCT	NP_000305.3:p.Gly282Ser
NM_000314.6:c.844_846delinsTCT	NP_000305.3:p.Gly282Ser
NM_001304717.2:c.1363_1365delinsTCT	NP_001291646.2:p.Gly455Ser
NM_001304718.1:c.253_255delinsTCT	NP_001291647.1:p.Gly85Ser
XM_006717926.2:c.799_801delinsTCT	XP_006717989.1:p.Gly267Ser
XM_011539981.1:c.844_846delinsTCT	XP_011538283.1:p.Gly282Ser
XM_011539982.1:c.748_750delinsTCT	XP_011538284.1:p.Gly250Ser
XR_945791.1:n.1414_1416delinsTCT
NM_000314.7:c.844_846delinsTCT	NP_000305.3:p.Gly282Ser
NM_001304717.5:c.1363_1365delinsTCT	NP_001291646.4:p.Gly455Ser
NM_001304718.2:c.253_255delinsTCT	NP_001291647.1:p.Gly85Ser
NM_000314.8:c.844_846delinsTCT MANE Select	NP_000305.3:p.Gly282Ser