Canonical Allele Identifier: CA995878737
Gene: AKT2 HGNC NCBI

Linked Data

dbSNP Id: rs2145449707

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.40285378_40285385del , CM000681.2:g.40285378_40285385del GRCh38
NC_000019.9:g.40791285_40791292del , CM000681.1:g.40791285_40791292del GRCh37
NC_000019.8:g.45483125_45483132del NCBI36
NG_012038.2:g.4974_4981del

Transcript Alleles

HGVS Amino-acid change
ENST00000392038.6:c.-289_-282del ENSP00000375892.2:n.-289_-282del
ENST00000424901.5:c.-289_-282del ENSP00000399532.2:n.-289_-282del
ENST00000578123.5:c.-85+63_-85+70del ENSP00000462022.1:n.-85+63_-85+70del
NM_001243027.2:c.-438_-431del NP_001229956.1:n.-438_-431del
NM_001243028.2:c.-345_-338del NP_001229957.1:n.-345_-338del
NM_001626.5:c.-289_-282del NP_001617.1:n.-289_-282del
XM_011526620.1:c.-85+63_-85+70del XP_011524922.1:n.-85+63_-85+70del