Canonical Allele Identifier: CA995878748
Gene: AKT2 HGNC NCBI

Linked Data

dbSNP Id: rs2077498488

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.40285384_40285385insCCCCCC , CM000681.2:g.40285384_40285385insCCCCCC GRCh38
NC_000019.9:g.40791291_40791292insCCCCCC , CM000681.1:g.40791291_40791292insCCCCCC GRCh37
NC_000019.8:g.45483131_45483132insCCCCCC NCBI36
NG_012038.2:g.4976_4977insGGGGGG

Transcript Alleles

HGVS Amino-acid change
ENST00000392038.6:c.-287_-286insGGGGGG ENSP00000375892.2:n.-287_-286insGGGGGG
ENST00000424901.5:c.-287_-286insGGGGGG ENSP00000399532.2:n.-287_-286insGGGGGG
ENST00000578123.5:c.-85+65_-85+66insGGGGGG ENSP00000462022.1:n.-85+65_-85+66insGGGGG...
NM_001243027.2:c.-436_-435insGGGGGG NP_001229956.1:n.-436_-435insGGGGGG
NM_001243028.2:c.-343_-342insGGGGGG NP_001229957.1:n.-343_-342insGGGGGG
NM_001626.5:c.-287_-286insGGGGGG NP_001617.1:n.-287_-286insGGGGGG
XM_011526620.1:c.-85+65_-85+66insGGGGGG XP_011524922.1:n.-85+65_-85+66insGGGGGG