Canonical Allele Identifier: CA882232846
Gene: AKT2 HGNC NCBI

Linked Data

dbSNP Id: rs1316701493
gnomAD v3: 19-40285347-C-CG
gnomAD v4: 19-40285347-C-CG
MyVariant Identifiers: chr19:g.40791254_40791255insG (hg19) chr19:g.40285347_40285348insG (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.40285349dup , CM000681.2:g.40285349dup GRCh38
NC_000019.9:g.40791256dup , CM000681.1:g.40791256dup GRCh37
NC_000019.8:g.45483096dup NCBI36
NG_012038.2:g.5011dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000391844.8:c.-298dup ENSP00000375719.4:n.-298dup
ENST00000392038.6:c.-252dup ENSP00000375892.2:n.-252dup
ENST00000424901.5:c.-252dup ENSP00000399532.2:n.-252dup
ENST00000578123.5:c.-85+100dup ENSP00000462022.1:n.-85+100dup
NM_001243027.2:c.-401dup NP_001229956.1:n.-401dup
NM_001243028.2:c.-308dup NP_001229957.1:n.-308dup
NM_001626.5:c.-252dup NP_001617.1:n.-252dup
XM_011526620.1:c.-85+100dup XP_011524922.1:n.-85+100dup
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