Canonical Allele Identifier: CA2814387113
Gene: AKT2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.40285351_40285352insGGG , CM000681.2:g.40285351_40285352insGGG GRCh38
NC_000019.9:g.40791258_40791259insGGG , CM000681.1:g.40791258_40791259insGGG GRCh37
NC_000019.8:g.45483098_45483099insGGG NCBI36
NG_012038.2:g.5007_5008insCCC

Transcript Alleles

HGVS Amino-acid Change
ENST00000391844.8:c.-302_-301insCCC ENSP00000375719.4:n.-302_-301insCCC
ENST00000392038.6:c.-256_-255insCCC ENSP00000375892.2:n.-256_-255insCCC
ENST00000424901.5:c.-256_-255insCCC ENSP00000399532.2:n.-256_-255insCCC
ENST00000578123.5:c.-85+96_-85+97insCCC ENSP00000462022.1:n.-85+96_-85+97insCCC
NM_001243027.2:c.-405_-404insCCC NP_001229956.1:n.-405_-404insCCC
NM_001243028.2:c.-312_-311insCCC NP_001229957.1:n.-312_-311insCCC
NM_001626.5:c.-256_-255insCCC NP_001617.1:n.-256_-255insCCC
XM_011526620.1:c.-85+96_-85+97insCCC XP_011524922.1:n.-85+96_-85+97insCCC