Canonical Allele Identifier: CA2335910071
Gene: AKT2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.40285379_40285382delinsCTTA , CM000681.2:g.40285379_40285382delinsCTTA GRCh38
NC_000019.9:g.40791286_40791289delinsCTTA , CM000681.1:g.40791286_40791289delinsCTTA GRCh37
NC_000019.8:g.45483126_45483129delinsCTTA NCBI36
NG_012038.2:g.4977_4980delinsTAAG

Transcript Alleles

HGVS Amino-acid change
ENST00000392038.6:c.-286_-283delinsTAAG ENSP00000375892.2:n.-286_-283delinsTAAG
ENST00000424901.5:c.-286_-283delinsTAAG ENSP00000399532.2:n.-286_-283delinsTAAG
ENST00000578123.5:c.-85+66_-85+69delinsTAAG ENSP00000462022.1:n.-85+66_-85+69delinsTA...
NM_001243027.2:c.-435_-432delinsTAAG NP_001229956.1:n.-435_-432delinsTAAG
NM_001243028.2:c.-342_-339delinsTAAG NP_001229957.1:n.-342_-339delinsTAAG
NM_001626.5:c.-286_-283delinsTAAG NP_001617.1:n.-286_-283delinsTAAG
XM_011526620.1:c.-85+66_-85+69delinsTAAG XP_011524922.1:n.-85+66_-85+69delinsTAAG