Canonical Allele Identifier: CA2335910041
Gene: AKT2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.40285358_40285359delinsGC , CM000681.2:g.40285358_40285359delinsGC GRCh38
NC_000019.9:g.40791265_40791266delinsGC , CM000681.1:g.40791265_40791266delinsGC GRCh37
NC_000019.8:g.45483105_45483106delinsGC NCBI36
NG_012038.2:g.5000_5001delinsGC

Transcript Alleles

HGVS Amino-acid Change
ENST00000391844.8:c.-309_-308delinsGC ENSP00000375719.4:n.-309_-308delinsGC
ENST00000392038.6:c.-263_-262delinsGC ENSP00000375892.2:n.-263_-262delinsGC
ENST00000424901.5:c.-263_-262delinsGC ENSP00000399532.2:n.-263_-262delinsGC
ENST00000578123.5:c.-85+89_-85+90delinsGC ENSP00000462022.1:n.-85+89_-85+90delinsGC
NM_001243027.2:c.-412_-411delinsGC NP_001229956.1:n.-412_-411delinsGC
NM_001243028.2:c.-319_-318delinsGC NP_001229957.1:n.-319_-318delinsGC
NM_001626.5:c.-263_-262delinsGC NP_001617.1:n.-263_-262delinsGC
XM_011526620.1:c.-85+89_-85+90delinsGC XP_011524922.1:n.-85+89_-85+90delinsGC