Canonical Allele Identifier: CA2814387127
Gene: AKT2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.40285377_40285378insTTTT , CM000681.2:g.40285377_40285378insTTTT GRCh38
NC_000019.9:g.40791284_40791285insTTTT , CM000681.1:g.40791284_40791285insTTTT GRCh37
NC_000019.8:g.45483124_45483125insTTTT NCBI36
NG_012038.2:g.4981_4982insAAAA

Transcript Alleles

HGVS Amino-acid Change
ENST00000392038.6:c.-282_-281insAAAA ENSP00000375892.2:n.-282_-281insAAAA
ENST00000424901.5:c.-282_-281insAAAA ENSP00000399532.2:n.-282_-281insAAAA
ENST00000578123.5:c.-85+70_-85+71insAAAA ENSP00000462022.1:n.-85+70_-85+71insAAAA
NM_001243027.2:c.-431_-430insAAAA NP_001229956.1:n.-431_-430insAAAA
NM_001243028.2:c.-338_-337insAAAA NP_001229957.1:n.-338_-337insAAAA
NM_001626.5:c.-282_-281insAAAA NP_001617.1:n.-282_-281insAAAA
XM_011526620.1:c.-85+70_-85+71insAAAA XP_011524922.1:n.-85+70_-85+71insAAAA