Canonical Allele Identifier: CA1926142888

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87863326_87863328delinsGCC , CM000672.2:g.87863326_87863328delinsGCC GRCh38
NC_000010.10:g.89623083_89623085delinsGCC , CM000672.1:g.89623083_89623085delinsGCC GRCh37
NC_000010.9:g.89613063_89613065delinsGCC NCBI36
NG_007466.2:g.4889_4891delinsGCC , LRG_311:g.4889_4891delinsGCC
NG_033079.1:g.5110_5112delinsGGC

Transcript Alleles

HGVS Amino-acid Change
ENST00000706954.1:c.-17+684_-17+686delinsGCC (PTEN) ENSP00000516674.1:n.-17+684_-17+686delinsGCC
ENST00000688308.1:c.-17+213_-17+215delinsGCC (PTEN) ENSP00000508752.1:n.-17+213_-17+215delinsGCC
ENST00000445946.5:c.-841_-839delinsGGC (KLLN) MANE Select ENSP00000392204.2:n.-841_-839delinsGGC
ENST00000371953.7:c.-1144_-1142delinsGCC (PTEN) ENSP00000361021.3:n.-1144_-1142delinsGCC
ENST00000445946.3:c.-841_-839delinsGGC (KLLN) ENSP00000392204.2:n.-841_-839delinsGGC
NM_001126049.1:c.-841_-839delinsGGC (KLLN) NP_001119521.1:n.-841_-839delinsGGC
NM_001126049.2:c.-841_-839delinsGGC (KLLN) MANE Select NP_001119521.1:n.-841_-839delinsGGC