Canonical Allele Identifier: CA1926142739

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87863149G= , CM000672.2:g.87863149G= GRCh38
NC_000010.10:g.89622906G= , CM000672.1:g.89622906G= GRCh37
NC_000010.9:g.89612886G= NCBI36
NG_007466.2:g.4712G= , LRG_311:g.4712G=
NG_033079.1:g.5289C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000706954.1:c.-17+507G= (PTEN) ENSP00000516674.1:n.-17+507G=
ENST00000688308.1:c.-17+36G= (PTEN) ENSP00000508752.1:n.-17+36G=
ENST00000445946.5:c.-662C= (KLLN) MANE Select ENSP00000392204.2:n.-662C=
ENST00000371953.7:c.-1321G= (PTEN) ENSP00000361021.3:n.-1321G=
ENST00000445946.3:c.-662C= (KLLN) ENSP00000392204.2:n.-662C=
NM_001126049.1:c.-662C= (KLLN) NP_001119521.1:n.-662C=
NM_001126049.2:c.-662C= (KLLN) MANE Select NP_001119521.1:n.-662C=