Canonical Allele Identifier: CA2335910067
Gene: AKT2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.40285377_40285382delinsCGCTTA , CM000681.2:g.40285377_40285382delinsCGCTTA GRCh38
NC_000019.9:g.40791284_40791289delinsCGCTTA , CM000681.1:g.40791284_40791289delinsCGCTTA GRCh37
NC_000019.8:g.45483124_45483129delinsCGCTTA NCBI36
NG_012038.2:g.4977_4982delinsTAAGCG

Transcript Alleles

HGVS Amino-acid Change
ENST00000392038.6:c.-286_-281delinsTAAGCG ENSP00000375892.2:n.-286_-281delinsTAAGCG
ENST00000424901.5:c.-286_-281delinsTAAGCG ENSP00000399532.2:n.-286_-281delinsTAAGCG
ENST00000578123.5:c.-85+66_-85+71delinsTAAGCG ENSP00000462022.1:n.-85+66_-85+71delinsTAAGCG
NM_001243027.2:c.-435_-430delinsTAAGCG NP_001229956.1:n.-435_-430delinsTAAGCG
NM_001243028.2:c.-342_-337delinsTAAGCG NP_001229957.1:n.-342_-337delinsTAAGCG
NM_001626.5:c.-286_-281delinsTAAGCG NP_001617.1:n.-286_-281delinsTAAGCG
XM_011526620.1:c.-85+66_-85+71delinsTAAGCG XP_011524922.1:n.-85+66_-85+71delinsTAAGCG