Canonical Allele Identifier: CA891834864

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87960937_87960938delinsCT , CM000672.2:g.87960937_87960938delinsCT	GRCh38
NC_000010.10:g.89720694_89720695delinsCT , CM000672.1:g.89720694_89720695delinsCT	GRCh37
NC_000010.9:g.89710674_89710675delinsCT	NCBI36
NG_007466.2:g.102499_102500delinsCT , LRG_311:g.102499_102500delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.938_939delinsCT	ENSP00000514759.2:p.Gly313Ala
ENST00000710265.1:c.845_846delinsCT	ENSP00000518161.1:p.Gly282Ala
ENST00000472832.3:c.845_846delinsCT	ENSP00000483066.2:p.Gly282Ala
ENST00000688158.2:n.1580_1581delinsCT
ENST00000688922.2:c.*675_*676delinsCT	ENSP00000508742.2:n.*675_*676delinsCT
ENST00000700021.1:c.800_801delinsCT	ENSP00000514757.1:p.Gly267Ala
ENST00000700022.1:c.*184_*185delinsCT	ENSP00000514758.1:n.*184_*185delinsCT
ENST00000700023.1:n.2003_2004delinsCT
ENST00000700024.1:n.2237_2238delinsCT
ENST00000700025.1:n.1614_1615delinsCT
ENST00000700026.1:n.482_483delinsCT
ENST00000700029.1:c.772_773delinsCT
ENST00000706954.1:c.845_846delinsCT	ENSP00000516674.1:p.Gly282Ala
ENST00000706955.1:c.*880_*881delinsCT	ENSP00000516675.1:n.*880_*881delinsCT
ENST00000686459.1:c.*431_*432delinsCT	ENSP00000508909.1:n.*431_*432delinsCT
ENST00000688158.1:c.*956_*957delinsCT	ENSP00000509254.1:n.*956_*957delinsCT
ENST00000688308.1:c.845_846delinsCT	ENSP00000508752.1:p.Gly282Ala
ENST00000688922.1:c.766_767delinsCT
ENST00000693560.1:c.1364_1365delinsCT	ENSP00000509861.1:p.Gly455Ala
ENST00000371953.8:c.845_846delinsCT MANE Select	ENSP00000361021.3:p.Gly282Ala
ENST00000371953.7:c.845_846delinsCT	ENSP00000361021.3:p.Gly282Ala
ENST00000472832.2:c.272_273delinsCT	ENSP00000483066.1:p.Gly91Ala
NM_000314.5:c.845_846delinsCT	NP_000305.3:p.Gly282Ala
NM_000314.6:c.845_846delinsCT	NP_000305.3:p.Gly282Ala
NM_001304717.2:c.1364_1365delinsCT	NP_001291646.2:p.Gly455Ala
NM_001304718.1:c.254_255delinsCT	NP_001291647.1:p.Gly85Ala
XM_006717926.2:c.800_801delinsCT	XP_006717989.1:p.Gly267Ala
XM_011539981.1:c.845_846delinsCT	XP_011538283.1:p.Gly282Ala
XM_011539982.1:c.749_750delinsCT	XP_011538284.1:p.Gly250Ala
XR_945791.1:n.1415_1416delinsCT
NM_000314.7:c.845_846delinsCT	NP_000305.3:p.Gly282Ala
NM_001304717.5:c.1364_1365delinsCT	NP_001291646.4:p.Gly455Ala
NM_001304718.2:c.254_255delinsCT	NP_001291647.1:p.Gly85Ala
NM_000314.8:c.845_846delinsCT MANE Select	NP_000305.3:p.Gly282Ala