Canonical Allele Identifier: CA2335910079
Gene: AKT2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.40285386C= , CM000681.2:g.40285386C= GRCh38
NC_000019.9:g.40791293C= , CM000681.1:g.40791293C= GRCh37
NC_000019.8:g.45483133C= NCBI36
NG_012038.2:g.4973G=

Transcript Alleles

HGVS Amino-acid change
ENST00000392038.6:c.-290G= ENSP00000375892.2:n.-290G=
ENST00000424901.5:c.-290G= ENSP00000399532.2:n.-290G=
ENST00000578123.5:c.-85+62G= ENSP00000462022.1:n.-85+62G=
NM_001243027.2:c.-439G= NP_001229956.1:n.-439G=
NM_001243028.2:c.-346G= NP_001229957.1:n.-346G=
NM_001626.5:c.-290G= NP_001617.1:n.-290G=
XM_011526620.1:c.-85+62G= XP_011524922.1:n.-85+62G=