Canonical Allele Identifier: CA2335910042
Gene: AKT2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.40285358G= , CM000681.2:g.40285358G= GRCh38
NC_000019.9:g.40791265G= , CM000681.1:g.40791265G= GRCh37
NC_000019.8:g.45483105G= NCBI36
NG_012038.2:g.5001C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000391844.8:c.-308C= ENSP00000375719.4:n.-308C=
ENST00000392038.6:c.-262C= ENSP00000375892.2:n.-262C=
ENST00000424901.5:c.-262C= ENSP00000399532.2:n.-262C=
ENST00000578123.5:c.-85+90C= ENSP00000462022.1:n.-85+90C=
NM_001243027.2:c.-411C= NP_001229956.1:n.-411C=
NM_001243028.2:c.-318C= NP_001229957.1:n.-318C=
NM_001626.5:c.-262C= NP_001617.1:n.-262C=
XM_011526620.1:c.-85+90C= XP_011524922.1:n.-85+90C=