Canonical Allele Identifier: CA1926143010

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87863461C= , CM000672.2:g.87863461C= GRCh38
NC_000010.10:g.89623218C= , CM000672.1:g.89623218C= GRCh37
NC_000010.9:g.89613198C= NCBI36
NG_007466.2:g.5024C= , LRG_311:g.5024C=
NG_033079.1:g.4977G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000706954.1:c.-17+819C= (PTEN) ENSP00000516674.1:n.-17+819C=
ENST00000688308.1:c.-17+348C= (PTEN) ENSP00000508752.1:n.-17+348C=
ENST00000693560.1:c.-489C= (PTEN) ENSP00000509861.1:n.-489C=
ENST00000445946.5:c.-974G= (KLLN) MANE Select ENSP00000392204.2:n.-974G=
ENST00000371953.7:c.-1009C= (PTEN) ENSP00000361021.3:n.-1009C=
ENST00000610634.1:c.-1111C= (PTEN) ENSP00000477517.1:n.-1111C=
NM_000314.5:c.-1008C= (PTEN) NP_000305.3:n.-1008C=
NM_000314.6:c.-1008C= (PTEN) NP_000305.3:n.-1008C=
NM_001304717.2:c.-489C= (PTEN) NP_001291646.2:n.-489C=
NM_001304718.1:c.-1713C= (PTEN) NP_001291647.1:n.-1713C=
NM_001126049.2:c.-974G= (KLLN) MANE Select NP_001119521.1:n.-974G=