Canonical Allele Identifier: CA8217376
Gene: FOXF1 HGNC NCBI

Linked Data

dbSNP Id: rs746392936
ExAC: 16:86544466 C / CCA
gnomAD v2: 16-86544466-C-CCA
gnomAD v3: 16-86510860-C-CCA
gnomAD v4: 16-86510860-C-CCA
MyVariant Identifiers: chr16:g.86544466_86544467insCA (hg19) chr16:g.86510860_86510861insCA (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.86510863_86510864dup , CM000678.2:g.86510863_86510864dup GRCh38
NC_000016.9:g.86544469_86544470dup , CM000678.1:g.86544469_86544470dup GRCh37
NC_000016.8:g.85101970_85101971dup NCBI36
NG_016273.1:g.5337_5338dup

Transcript Alleles

HGVS Amino-acid change
ENST00000262426.6:c.294_295dup MANE Select ENSP00000262426.4:p.Asn99ThrfsTer?
ENST00000262426.5:c.294_295dup ENSP00000262426.4:p.Asn99ThrfsTer?
NM_001451.2:c.294_295dup NP_001442.2:p.Asn99ThrfsTer?
NM_001451.3:c.294_295dup MANE Select NP_001442.2:p.Asn99ThrfsTer?
Search 100 bp 5'
Search 100 bp 3'