Canonical Allele Identifier: CA2335910081
Gene: AKT2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.40285387C= , CM000681.2:g.40285387C= GRCh38
NC_000019.9:g.40791294C= , CM000681.1:g.40791294C= GRCh37
NC_000019.8:g.45483134C= NCBI36
NG_012038.2:g.4972G=

Transcript Alleles

HGVS Amino-acid change
ENST00000392038.6:c.-291G= ENSP00000375892.2:n.-291G=
ENST00000424901.5:c.-291G= ENSP00000399532.2:n.-291G=
ENST00000578123.5:c.-85+61G= ENSP00000462022.1:n.-85+61G=
NM_001243027.2:c.-440G= NP_001229956.1:n.-440G=
NM_001243028.2:c.-347G= NP_001229957.1:n.-347G=
NM_001626.5:c.-291G= NP_001617.1:n.-291G=
XM_011526620.1:c.-85+61G= XP_011524922.1:n.-85+61G=