Canonical Allele Identifier: CA2335910050
Gene: AKT2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.40285364T= , CM000681.2:g.40285364T= GRCh38
NC_000019.9:g.40791271T= , CM000681.1:g.40791271T= GRCh37
NC_000019.8:g.45483111T= NCBI36
NG_012038.2:g.4995A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000391844.8:c.-314A= ENSP00000375719.4:n.-314A=
ENST00000392038.6:c.-268A= ENSP00000375892.2:n.-268A=
ENST00000424901.5:c.-268A= ENSP00000399532.2:n.-268A=
ENST00000578123.5:c.-85+84A= ENSP00000462022.1:n.-85+84A=
NM_001243027.2:c.-417A= NP_001229956.1:n.-417A=
NM_001243028.2:c.-324A= NP_001229957.1:n.-324A=
NM_001626.5:c.-268A= NP_001617.1:n.-268A=
XM_011526620.1:c.-85+84A= XP_011524922.1:n.-85+84A=