Canonical Allele Identifier: CA1926142683

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87863056C= , CM000672.2:g.87863056C= GRCh38
NC_000010.10:g.89622813C= , CM000672.1:g.89622813C= GRCh37
NC_000010.9:g.89612793C= NCBI36
NG_007466.2:g.4619C= , LRG_311:g.4619C=
NG_033079.1:g.5382G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000706954.1:c.-17+414C= (PTEN) ENSP00000516674.1:n.-17+414C=
ENST00000688308.1:c.-74C= (PTEN) ENSP00000508752.1:n.-74C=
ENST00000445946.5:c.-569G= (KLLN) MANE Select ENSP00000392204.2:n.-569G=
ENST00000445946.3:c.-569G= (KLLN) ENSP00000392204.2:n.-569G=
NM_001126049.1:c.-569G= (KLLN) NP_001119521.1:n.-569G=
NM_001126049.2:c.-569G= (KLLN) MANE Select NP_001119521.1:n.-569G=