Canonical Allele Identifier: CA995878746
Gene: AKT2 HGNC NCBI

Linked Data

gnomAD v3: 19-40285382-A-ACCCC
gnomAD v4: 19-40285382-A-ACCCC
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.40285384_40285385insCCCC , CM000681.2:g.40285384_40285385insCCCC GRCh38
NC_000019.9:g.40791291_40791292insCCCC , CM000681.1:g.40791291_40791292insCCCC GRCh37
NC_000019.8:g.45483131_45483132insCCCC NCBI36
NG_012038.2:g.4976_4977insGGGG

Transcript Alleles

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