Canonical Allele Identifier: CA1926143221

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87863705G= , CM000672.2:g.87863705G=	GRCh38
NC_000010.10:g.89623462G= , CM000672.1:g.89623462G=	GRCh37
NC_000010.9:g.89613442G=	NCBI36
NG_007466.2:g.5268G= , LRG_311:g.5268G=
NG_033079.1:g.4733C=

Transcript Alleles

HGVS	Amino-acid Change
NM_000314.8:c.-765G= MANE Select	NP_000305.3:n.-765G=
ENST00000371953.8:c.-765G= MANE Select	ENSP00000361021.3:n.-765G=
NM_000314.5:c.-764G=	NP_000305.3:n.-764G=
NM_000314.6:c.-764G=	NP_000305.3:n.-764G=
NM_000314.7:c.-764G=	NP_000305.3:n.-764G=
NM_001304717.2:c.-245G=	NP_001291646.2:n.-245G=
NM_001304717.5:c.-245G=	NP_001291646.4:n.-245G=
NM_001304718.1:c.-1469G=	NP_001291647.1:n.-1469G=
NM_001304718.2:c.-1469G=	NP_001291647.1:n.-1469G=
ENST00000371953.7:c.-765G=	ENSP00000361021.3:n.-765G=
ENST00000610634.1:c.-867G=	ENSP00000477517.1:n.-867G=
ENST00000688158.1:c.-765G=	ENSP00000509254.1:n.-765G=
ENST00000688308.1:c.-17+592G=	ENSP00000508752.1:n.-17+592G=
ENST00000693560.1:c.-245G=	ENSP00000509861.1:n.-245G=
ENST00000700029.2:c.-765G=	ENSP00000514759.2:n.-765G=
ENST00000706954.1:c.-16-749G=	ENSP00000516674.1:n.-16-749G=
ENST00000706955.1:c.-765G=	ENSP00000516675.1:n.-765G=
ENST00000710265.1:c.-765G=	ENSP00000518161.1:n.-765G=