Canonical Allele Identifier: CA2335910061
Gene: AKT2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.40285371A= , CM000681.2:g.40285371A= GRCh38
NC_000019.9:g.40791278A= , CM000681.1:g.40791278A= GRCh37
NC_000019.8:g.45483118A= NCBI36
NG_012038.2:g.4988T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000391844.8:c.-321T= ENSP00000375719.4:n.-321T=
ENST00000392038.6:c.-275T= ENSP00000375892.2:n.-275T=
ENST00000424901.5:c.-275T= ENSP00000399532.2:n.-275T=
ENST00000578123.5:c.-85+77T= ENSP00000462022.1:n.-85+77T=
NM_001243027.2:c.-424T= NP_001229956.1:n.-424T=
NM_001243028.2:c.-331T= NP_001229957.1:n.-331T=
NM_001626.5:c.-275T= NP_001617.1:n.-275T=
XM_011526620.1:c.-85+77T= XP_011524922.1:n.-85+77T=