Canonical Allele Identifier: CA1926142998

Gene: PTEN KLLN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87863444C= , CM000672.2:g.87863444C=	GRCh38
NC_000010.10:g.89623201C= , CM000672.1:g.89623201C=	GRCh37
NC_000010.9:g.89613181C=	NCBI36
NG_007466.2:g.5007C= , LRG_311:g.5007C=
NG_033079.1:g.4994G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000706954.1:c.-17+802C= (PTEN)	ENSP00000516674.1:n.-17+802C=
ENST00000688308.1:c.-17+331C= (PTEN)	ENSP00000508752.1:n.-17+331C=
ENST00000693560.1:c.-506C= (PTEN)	ENSP00000509861.1:n.-506C=
ENST00000445946.5:c.-957G= (KLLN) MANE Select	ENSP00000392204.2:n.-957G=
ENST00000371953.7:c.-1026C= (PTEN)	ENSP00000361021.3:n.-1026C=
ENST00000610634.1:c.-1128C= (PTEN)	ENSP00000477517.1:n.-1128C=
NM_000314.5:c.-1025C= (PTEN)	NP_000305.3:n.-1025C=
NM_000314.6:c.-1025C= (PTEN)	NP_000305.3:n.-1025C=
NM_001304717.2:c.-506C= (PTEN)	NP_001291646.2:n.-506C=
NM_001304718.1:c.-1730C= (PTEN)	NP_001291647.1:n.-1730C=
NM_001126049.2:c.-957G= (KLLN) MANE Select	NP_001119521.1:n.-957G=