Canonical Allele Identifier: CA2335910076
Gene: AKT2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.40285382A= , CM000681.2:g.40285382A= GRCh38
NC_000019.9:g.40791289A= , CM000681.1:g.40791289A= GRCh37
NC_000019.8:g.45483129A= NCBI36
NG_012038.2:g.4977T=

Transcript Alleles

HGVS Amino-acid change
ENST00000392038.6:c.-286T= ENSP00000375892.2:n.-286T=
ENST00000424901.5:c.-286T= ENSP00000399532.2:n.-286T=
ENST00000578123.5:c.-85+66T= ENSP00000462022.1:n.-85+66T=
NM_001243027.2:c.-435T= NP_001229956.1:n.-435T=
NM_001243028.2:c.-342T= NP_001229957.1:n.-342T=
NM_001626.5:c.-286T= NP_001617.1:n.-286T=
XM_011526620.1:c.-85+66T= XP_011524922.1:n.-85+66T=