Canonical Allele Identifier: CA2585108909
Gene: AKT2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.40285309_40285311del , CM000681.2:g.40285309_40285311del GRCh38
NC_000019.9:g.40791216_40791218del , CM000681.1:g.40791216_40791218del GRCh37
NC_000019.8:g.45483056_45483058del NCBI36
NG_012038.2:g.5050_5052del

Transcript Alleles

HGVS Amino-acid Change
ENST00000392038.7:c.-213_-211del MANE Select ENSP00000375892.2:n.-213_-211del
ENST00000391844.8:c.-259_-257del ENSP00000375719.4:n.-259_-257del
ENST00000392038.6:c.-213_-211del ENSP00000375892.2:n.-213_-211del
ENST00000424901.5:c.-213_-211del ENSP00000399532.2:n.-213_-211del
ENST00000578123.5:c.-85+139_-85+141del ENSP00000462022.1:n.-85+139_-85+141del
ENST00000579047.5:c.-269_-267del ENSP00000471369.1:n.-269_-267del
ENST00000584288.5:c.-352_-350del ENSP00000462469.1:n.-352_-350del
NM_001243027.2:c.-362_-360del NP_001229956.1:n.-362_-360del
NM_001243028.2:c.-269_-267del NP_001229957.1:n.-269_-267del
NM_001626.5:c.-213_-211del NP_001617.1:n.-213_-211del
XM_011526620.1:c.-85+139_-85+141del XP_011524922.1:n.-85+139_-85+141del
XM_011526622.1:c.-213_-211del XP_011524924.1:n.-213_-211del
XM_011526622.2:c.-213_-211del XP_011524924.1:n.-213_-211del
XM_024451417.1:c.-213_-211del XP_024307185.1:n.-213_-211del
NM_001626.6:c.-213_-211del MANE Select NP_001617.1:n.-213_-211del
NM_001243027.3:c.-362_-360del NP_001229956.1:n.-362_-360del
NM_001243028.3:c.-269_-267del NP_001229957.1:n.-269_-267del