Canonical Allele Identifier: CA995878642
Gene: AKT2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.40285350_40285351insACC , CM000681.2:g.40285350_40285351insACC GRCh38
NC_000019.9:g.40791257_40791258insACC , CM000681.1:g.40791257_40791258insACC GRCh37
NC_000019.8:g.45483097_45483098insACC NCBI36
NG_012038.2:g.5009_5010insGTG

Transcript Alleles

HGVS Amino-acid Change
ENST00000391844.8:c.-300_-299insGTG ENSP00000375719.4:n.-300_-299insGTG
ENST00000392038.6:c.-254_-253insGTG ENSP00000375892.2:n.-254_-253insGTG
ENST00000424901.5:c.-254_-253insGTG ENSP00000399532.2:n.-254_-253insGTG
ENST00000578123.5:c.-85+98_-85+99insGTG ENSP00000462022.1:n.-85+98_-85+99insGTG
NM_001243027.2:c.-403_-402insGTG NP_001229956.1:n.-403_-402insGTG
NM_001243028.2:c.-310_-309insGTG NP_001229957.1:n.-310_-309insGTG
NM_001626.5:c.-254_-253insGTG NP_001617.1:n.-254_-253insGTG
XM_011526620.1:c.-85+98_-85+99insGTG XP_011524922.1:n.-85+98_-85+99insGTG