Canonical Allele Identifier: CA1926142723

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87863119C= , CM000672.2:g.87863119C= GRCh38
NC_000010.10:g.89622876C= , CM000672.1:g.89622876C= GRCh37
NC_000010.9:g.89612856C= NCBI36
NG_007466.2:g.4682C= , LRG_311:g.4682C=
NG_033079.1:g.5319G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000706954.1:c.-17+477C= (PTEN) ENSP00000516674.1:n.-17+477C=
ENST00000688308.1:c.-17+6C= (PTEN) ENSP00000508752.1:n.-17+6C=
ENST00000445946.5:c.-632G= (KLLN) MANE Select ENSP00000392204.2:n.-632G=
ENST00000371953.7:c.-1351C= (PTEN) ENSP00000361021.3:n.-1351C=
ENST00000445946.3:c.-632G= (KLLN) ENSP00000392204.2:n.-632G=
NM_001126049.1:c.-632G= (KLLN) NP_001119521.1:n.-632G=
NM_001126049.2:c.-632G= (KLLN) MANE Select NP_001119521.1:n.-632G=