Canonical Allele Identifier: CA1926190001

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87960969G= , CM000672.2:g.87960969G=	GRCh38
NC_000010.10:g.89720726G= , CM000672.1:g.89720726G=	GRCh37
NC_000010.9:g.89710706G=	NCBI36
NG_007466.2:g.102531G= , LRG_311:g.102531G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000700029.2:c.970G=	ENSP00000514759.2:p.Gly324=
ENST00000710265.1:c.877G=	ENSP00000518161.1:p.Gly293=
ENST00000472832.3:c.877G=	ENSP00000483066.2:p.Gly293=
ENST00000688158.2:n.1612G=
ENST00000688922.2:c.*707G=	ENSP00000508742.2:n.*707G=
ENST00000700021.1:c.832G=	ENSP00000514757.1:p.Gly278=
ENST00000700022.1:c.*216G=	ENSP00000514758.1:n.*216G=
ENST00000700023.1:n.2035G=
ENST00000700024.1:n.2269G=
ENST00000700025.1:n.1646G=
ENST00000700026.1:n.514G=
ENST00000700029.1:c.804G=
ENST00000706954.1:c.877G=	ENSP00000516674.1:p.Gly293=
ENST00000706955.1:c.*912G=	ENSP00000516675.1:n.*912G=
ENST00000686459.1:c.*463G=	ENSP00000508909.1:n.*463G=
ENST00000688158.1:c.*988G=	ENSP00000509254.1:n.*988G=
ENST00000688308.1:c.877G=	ENSP00000508752.1:p.Gly293=
ENST00000688922.1:c.798G=
ENST00000693560.1:c.1396G=	ENSP00000509861.1:p.Gly466=
ENST00000371953.8:c.877G= MANE Select	ENSP00000361021.3:p.Gly293=
ENST00000371953.7:c.877G=	ENSP00000361021.3:p.Gly293=
ENST00000472832.2:c.304G=	ENSP00000483066.1:p.Gly102=
NM_000314.5:c.877G=	NP_000305.3:p.Gly293=
NM_000314.6:c.877G=	NP_000305.3:p.Gly293=
NM_001304717.2:c.1396G=	NP_001291646.2:p.Gly466=
NM_001304718.1:c.286G=	NP_001291647.1:p.Gly96=
XM_006717926.2:c.832G=	XP_006717989.1:p.Gly278=
XM_011539981.1:c.877G=	XP_011538283.1:p.Gly293=
XM_011539982.1:c.781G=	XP_011538284.1:p.Gly261=
XR_945791.1:n.1447G=
NM_000314.7:c.877G=	NP_000305.3:p.Gly293=
NM_001304717.5:c.1396G=	NP_001291646.4:p.Gly466=
NM_001304718.2:c.286G=	NP_001291647.1:p.Gly96=
NM_000314.8:c.877G= MANE Select	NP_000305.3:p.Gly293=