Canonical Allele Identifier: CA633110968
Gene: AKT2 HGNC NCBI

Linked Data

dbSNP Id: rs1244908199
gnomAD v2: 19-40791262-C-CCCGCCCCCTCCCCCCAGCCCCCGCTTA
gnomAD v3: 19-40285355-C-CCCGCCCCCTCCCCCCAGCCCCCGCTTA
gnomAD v4: 19-40285355-C-CCCGCCCCCTCCCCCCAGCCCCCGCTTA
MyVariant Identifiers: chr19:g.40791262_40791263insCCGCCCCCTCCCCCCAGCCCCCGCTTA (hg19) chr19:g.40285355_40285356insCCGCCCCCTCCCCCCAGCCCCCGCTTA (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.40285368_40285394dup , CM000681.2:g.40285368_40285394dup GRCh38
NC_000019.9:g.40791275_40791301dup , CM000681.1:g.40791275_40791301dup GRCh37
NC_000019.8:g.45483115_45483141dup NCBI36
NG_012038.2:g.4977_5003dup

Transcript Alleles

HGVS Amino-acid change
ENST00000392038.6:c.-286_-260dup ENSP00000375892.2:n.-286_-260dup
ENST00000424901.5:c.-286_-260dup ENSP00000399532.2:n.-286_-260dup
ENST00000578123.5:c.-85+66_-85+92dup ENSP00000462022.1:n.-85+66_-85+92dup
NM_001243027.2:c.-435_-409dup NP_001229956.1:n.-435_-409dup
NM_001243028.2:c.-342_-316dup NP_001229957.1:n.-342_-316dup
NM_001626.5:c.-286_-260dup NP_001617.1:n.-286_-260dup
XM_011526620.1:c.-85+66_-85+92dup XP_011524922.1:n.-85+66_-85+92dup
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