Canonical Allele Identifier: CA1926142905

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87863341_87863342delinsAC , CM000672.2:g.87863341_87863342delinsAC GRCh38
NC_000010.10:g.89623098_89623099delinsAC , CM000672.1:g.89623098_89623099delinsAC GRCh37
NC_000010.9:g.89613078_89613079delinsAC NCBI36
NG_007466.2:g.4904_4905delinsAC , LRG_311:g.4904_4905delinsAC
NG_033079.1:g.5096_5097delinsGT

Transcript Alleles

HGVS Amino-acid Change
ENST00000706954.1:c.-17+699_-17+700delinsAC (PTEN) ENSP00000516674.1:n.-17+699_-17+700delinsAC
ENST00000688308.1:c.-17+228_-17+229delinsAC (PTEN) ENSP00000508752.1:n.-17+228_-17+229delinsAC
ENST00000445946.5:c.-855_-854delinsGT (KLLN) MANE Select ENSP00000392204.2:n.-855_-854delinsGT
ENST00000371953.7:c.-1129_-1128delinsAC (PTEN) ENSP00000361021.3:n.-1129_-1128delinsAC
ENST00000445946.3:c.-855_-854delinsGT (KLLN) ENSP00000392204.2:n.-855_-854delinsGT
NM_001126049.1:c.-855_-854delinsGT (KLLN) NP_001119521.1:n.-855_-854delinsGT
NM_001126049.2:c.-855_-854delinsGT (KLLN) MANE Select NP_001119521.1:n.-855_-854delinsGT