Canonical Allele Identifier: CA1926142823

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87863259C= , CM000672.2:g.87863259C= GRCh38
NC_000010.10:g.89623016C= , CM000672.1:g.89623016C= GRCh37
NC_000010.9:g.89612996C= NCBI36
NG_007466.2:g.4822C= , LRG_311:g.4822C=
NG_033079.1:g.5179G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000706954.1:c.-17+617C= (PTEN) ENSP00000516674.1:n.-17+617C=
ENST00000688308.1:c.-17+146C= (PTEN) ENSP00000508752.1:n.-17+146C=
ENST00000445946.5:c.-772G= (KLLN) MANE Select ENSP00000392204.2:n.-772G=
ENST00000371953.7:c.-1211C= (PTEN) ENSP00000361021.3:n.-1211C=
ENST00000445946.3:c.-772G= (KLLN) ENSP00000392204.2:n.-772G=
NM_001126049.1:c.-772G= (KLLN) NP_001119521.1:n.-772G=
NM_001126049.2:c.-772G= (KLLN) MANE Select NP_001119521.1:n.-772G=