Canonical Allele Identifier: CA1926142994

Gene: PTEN KLLN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87863440T= , CM000672.2:g.87863440T=	GRCh38
NC_000010.10:g.89623197T= , CM000672.1:g.89623197T=	GRCh37
NC_000010.9:g.89613177T=	NCBI36
NG_007466.2:g.5003T= , LRG_311:g.5003T=
NG_033079.1:g.4998A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000706954.1:c.-17+798T= (PTEN)	ENSP00000516674.1:n.-17+798T=
ENST00000688308.1:c.-17+327T= (PTEN)	ENSP00000508752.1:n.-17+327T=
ENST00000693560.1:c.-510T= (PTEN)	ENSP00000509861.1:n.-510T=
ENST00000445946.5:c.-953A= (KLLN) MANE Select	ENSP00000392204.2:n.-953A=
ENST00000371953.7:c.-1030T= (PTEN)	ENSP00000361021.3:n.-1030T=
ENST00000610634.1:c.-1132T= (PTEN)	ENSP00000477517.1:n.-1132T=
NM_000314.5:c.-1029T= (PTEN)	NP_000305.3:n.-1029T=
NM_000314.6:c.-1029T= (PTEN)	NP_000305.3:n.-1029T=
NM_001304717.2:c.-510T= (PTEN)	NP_001291646.2:n.-510T=
NM_001304718.1:c.-1734T= (PTEN)	NP_001291647.1:n.-1734T=
NM_001126049.2:c.-953A= (KLLN) MANE Select	NP_001119521.1:n.-953A=