Canonical Allele Identifier: CA1926142924

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87863364G= , CM000672.2:g.87863364G= GRCh38
NC_000010.10:g.89623121G= , CM000672.1:g.89623121G= GRCh37
NC_000010.9:g.89613101G= NCBI36
NG_007466.2:g.4927G= , LRG_311:g.4927G=
NG_033079.1:g.5074C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000706954.1:c.-17+722G= (PTEN) ENSP00000516674.1:n.-17+722G=
ENST00000688308.1:c.-17+251G= (PTEN) ENSP00000508752.1:n.-17+251G=
ENST00000445946.5:c.-877C= (KLLN) MANE Select ENSP00000392204.2:n.-877C=
ENST00000371953.7:c.-1106G= (PTEN) ENSP00000361021.3:n.-1106G=
ENST00000445946.3:c.-877C= (KLLN) ENSP00000392204.2:n.-877C=
NM_001126049.1:c.-877C= (KLLN) NP_001119521.1:n.-877C=
NM_001126049.2:c.-877C= (KLLN) MANE Select NP_001119521.1:n.-877C=