Canonical Allele Identifier: CA2335910046
Gene: AKT2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.40285362C= , CM000681.2:g.40285362C= GRCh38
NC_000019.9:g.40791269C= , CM000681.1:g.40791269C= GRCh37
NC_000019.8:g.45483109C= NCBI36
NG_012038.2:g.4997G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000391844.8:c.-312G= ENSP00000375719.4:n.-312G=
ENST00000392038.6:c.-266G= ENSP00000375892.2:n.-266G=
ENST00000424901.5:c.-266G= ENSP00000399532.2:n.-266G=
ENST00000578123.5:c.-85+86G= ENSP00000462022.1:n.-85+86G=
NM_001243027.2:c.-415G= NP_001229956.1:n.-415G=
NM_001243028.2:c.-322G= NP_001229957.1:n.-322G=
NM_001626.5:c.-266G= NP_001617.1:n.-266G=
XM_011526620.1:c.-85+86G= XP_011524922.1:n.-85+86G=