Canonical Allele Identifier: CA3949216
Gene: FOXO3 HGNC NCBI

Linked Data

dbSNP Id: rs755180768
ExAC: 6:108882791 T / TGCA
gnomAD v2: 6-108882791-T-TGCA
gnomAD v4: 6-108561588-T-TGCA
MyVariant Identifiers: chr6:g.108882791_108882792insGCA (hg19) chr6:g.108561588_108561589insGCA (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.108561591_108561593dup , CM000668.2:g.108561591_108561593dup GRCh38
NC_000006.11:g.108882794_108882796dup , CM000668.1:g.108882794_108882796dup GRCh37
NC_000006.10:g.108989487_108989489dup NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000406360.2:c.383_385dup MANE Select ENSP00000385824.1:p.Gln128_Pro129insGln
ENST00000343882.10:c.383_385dup ENSP00000339527.6:p.Gln128_Pro129insGln
ENST00000406360.1:c.383_385dup ENSP00000385824.1:p.Gln128_Pro129insGln
NM_001455.3:c.383_385dup NP_001446.1:p.Gln128_Pro129insGln
NM_201559.2:c.383_385dup NP_963853.1:p.Gln128_Pro129insGln
NM_001455.4:c.383_385dup MANE Select NP_001446.1:p.Gln128_Pro129insGln
NM_201559.3:c.383_385dup NP_963853.1:p.Gln128_Pro129insGln
Search 100 bp 5'
Search 100 bp 3'