Canonical Allele Identifier: CA633110984
Gene: AKT2 HGNC NCBI

Linked Data

dbSNP Id: rs1600131887
gnomAD v2: 19-40791286-CTTA-C
gnomAD v3: 19-40285379-CTTA-C
gnomAD v4: 19-40285379-CTTA-C
MyVariant Identifiers: chr19:g.40791287_40791289del (hg19) chr19:g.40285380_40285382del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.40285380_40285382del , CM000681.2:g.40285380_40285382del GRCh38
NC_000019.9:g.40791287_40791289del , CM000681.1:g.40791287_40791289del GRCh37
NC_000019.8:g.45483127_45483129del NCBI36
NG_012038.2:g.4977_4979del

Transcript Alleles

HGVS Amino-acid change
ENST00000392038.6:c.-286_-284del ENSP00000375892.2:n.-286_-284del
ENST00000424901.5:c.-286_-284del ENSP00000399532.2:n.-286_-284del
ENST00000578123.5:c.-85+66_-85+68del ENSP00000462022.1:n.-85+66_-85+68del
NM_001243027.2:c.-435_-433del NP_001229956.1:n.-435_-433del
NM_001243028.2:c.-342_-340del NP_001229957.1:n.-342_-340del
NM_001626.5:c.-286_-284del NP_001617.1:n.-286_-284del
XM_011526620.1:c.-85+66_-85+68del XP_011524922.1:n.-85+66_-85+68del
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