Canonical Allele Identifier: CA2533512381
Gene: AKT2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.40285355_40285357dup , CM000681.2:g.40285355_40285357dup GRCh38
NC_000019.9:g.40791262_40791264dup , CM000681.1:g.40791262_40791264dup GRCh37
NC_000019.8:g.45483102_45483104dup NCBI36
NG_012038.2:g.5007_5009dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000391844.8:c.-302_-300dup ENSP00000375719.4:n.-302_-300dup
ENST00000392038.6:c.-256_-254dup ENSP00000375892.2:n.-256_-254dup
ENST00000424901.5:c.-256_-254dup ENSP00000399532.2:n.-256_-254dup
ENST00000578123.5:c.-85+96_-85+98dup ENSP00000462022.1:n.-85+96_-85+98dup
NM_001243027.2:c.-405_-403dup NP_001229956.1:n.-405_-403dup
NM_001243028.2:c.-312_-310dup NP_001229957.1:n.-312_-310dup
NM_001626.5:c.-256_-254dup NP_001617.1:n.-256_-254dup
XM_011526620.1:c.-85+96_-85+98dup XP_011524922.1:n.-85+96_-85+98dup