Canonical Allele Identifier: CA1926142867

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87863308_87863309delinsGG , CM000672.2:g.87863308_87863309delinsGG GRCh38
NC_000010.10:g.89623065_89623066delinsGG , CM000672.1:g.89623065_89623066delinsGG GRCh37
NC_000010.9:g.89613045_89613046delinsGG NCBI36
NG_007466.2:g.4871_4872delinsGG , LRG_311:g.4871_4872delinsGG
NG_033079.1:g.5129_5130delinsCC

Transcript Alleles

HGVS Amino-acid Change
ENST00000706954.1:c.-17+666_-17+667delinsGG (PTEN) ENSP00000516674.1:n.-17+666_-17+667delinsGG
ENST00000688308.1:c.-17+195_-17+196delinsGG (PTEN) ENSP00000508752.1:n.-17+195_-17+196delinsGG
ENST00000445946.5:c.-822_-821delinsCC (KLLN) MANE Select ENSP00000392204.2:n.-822_-821delinsCC
ENST00000371953.7:c.-1162_-1161delinsGG (PTEN) ENSP00000361021.3:n.-1162_-1161delinsGG
ENST00000445946.3:c.-822_-821delinsCC (KLLN) ENSP00000392204.2:n.-822_-821delinsCC
NM_001126049.1:c.-822_-821delinsCC (KLLN) NP_001119521.1:n.-822_-821delinsCC
NM_001126049.2:c.-822_-821delinsCC (KLLN) MANE Select NP_001119521.1:n.-822_-821delinsCC