Canonical Allele Identifier: CA2335910074
Gene: AKT2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.40285380T= , CM000681.2:g.40285380T= GRCh38
NC_000019.9:g.40791287T= , CM000681.1:g.40791287T= GRCh37
NC_000019.8:g.45483127T= NCBI36
NG_012038.2:g.4979A=

Transcript Alleles

HGVS Amino-acid change
ENST00000392038.6:c.-284A= ENSP00000375892.2:n.-284A=
ENST00000424901.5:c.-284A= ENSP00000399532.2:n.-284A=
ENST00000578123.5:c.-85+68A= ENSP00000462022.1:n.-85+68A=
NM_001243027.2:c.-433A= NP_001229956.1:n.-433A=
NM_001243028.2:c.-340A= NP_001229957.1:n.-340A=
NM_001626.5:c.-284A= NP_001617.1:n.-284A=
XM_011526620.1:c.-85+68A= XP_011524922.1:n.-85+68A=