Canonical Allele Identifier: CA2814387114
Gene: AKT2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.40285352C>T , CM000681.2:g.40285352C>T GRCh38
NC_000019.9:g.40791259C>T , CM000681.1:g.40791259C>T GRCh37
NC_000019.8:g.45483099C>T NCBI36
NG_012038.2:g.5007G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000391844.8:c.-302G>A ENSP00000375719.4:n.-302G>A
ENST00000392038.6:c.-256G>A ENSP00000375892.2:n.-256G>A
ENST00000424901.5:c.-256G>A ENSP00000399532.2:n.-256G>A
ENST00000578123.5:c.-85+96G>A ENSP00000462022.1:n.-85+96G>A
NM_001243027.2:c.-405G>A NP_001229956.1:n.-405G>A
NM_001243028.2:c.-312G>A NP_001229957.1:n.-312G>A
NM_001626.5:c.-256G>A NP_001617.1:n.-256G>A
XM_011526620.1:c.-85+96G>A XP_011524922.1:n.-85+96G>A