Canonical Allele Identifier: CA1926142999

Gene: PTEN KLLN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87863446C= , CM000672.2:g.87863446C=	GRCh38
NC_000010.10:g.89623203C= , CM000672.1:g.89623203C=	GRCh37
NC_000010.9:g.89613183C=	NCBI36
NG_007466.2:g.5009C= , LRG_311:g.5009C=
NG_033079.1:g.4992G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000706954.1:c.-17+804C= (PTEN)	ENSP00000516674.1:n.-17+804C=
ENST00000688308.1:c.-17+333C= (PTEN)	ENSP00000508752.1:n.-17+333C=
ENST00000693560.1:c.-504C= (PTEN)	ENSP00000509861.1:n.-504C=
ENST00000445946.5:c.-959G= (KLLN) MANE Select	ENSP00000392204.2:n.-959G=
ENST00000371953.7:c.-1024C= (PTEN)	ENSP00000361021.3:n.-1024C=
ENST00000610634.1:c.-1126C= (PTEN)	ENSP00000477517.1:n.-1126C=
NM_000314.5:c.-1023C= (PTEN)	NP_000305.3:n.-1023C=
NM_000314.6:c.-1023C= (PTEN)	NP_000305.3:n.-1023C=
NM_001304717.2:c.-504C= (PTEN)	NP_001291646.2:n.-504C=
NM_001304718.1:c.-1728C= (PTEN)	NP_001291647.1:n.-1728C=
NM_001126049.2:c.-959G= (KLLN) MANE Select	NP_001119521.1:n.-959G=