Canonical Allele Identifier: CA633110985
Gene: AKT2 HGNC NCBI

Linked Data

dbSNP Id: rs2145449721
gnomAD v2: 19-40791286-CTT-C
gnomAD v3: 19-40285379-CTT-C
gnomAD v4: 19-40285379-CTT-C
MyVariant Identifiers: chr19:g.40791287_40791289delinsA (hg19) chr19:g.40285380_40285382delinsA (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.40285380_40285381del , CM000681.2:g.40285380_40285381del GRCh38
NC_000019.9:g.40791287_40791288del , CM000681.1:g.40791287_40791288del GRCh37
NC_000019.8:g.45483127_45483128del NCBI36
NG_012038.2:g.4978_4979del

Transcript Alleles

HGVS Amino-acid change
ENST00000392038.6:c.-285_-284del ENSP00000375892.2:n.-285_-284del
ENST00000424901.5:c.-285_-284del ENSP00000399532.2:n.-285_-284del
ENST00000578123.5:c.-85+67_-85+68del ENSP00000462022.1:n.-85+67_-85+68del
NM_001243027.2:c.-434_-433del NP_001229956.1:n.-434_-433del
NM_001243028.2:c.-341_-340del NP_001229957.1:n.-341_-340del
NM_001626.5:c.-285_-284del NP_001617.1:n.-285_-284del
XM_011526620.1:c.-85+67_-85+68del XP_011524922.1:n.-85+67_-85+68del
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