Canonical Allele Identifier: CA961450268
Gene: FOXG1 HGNC NCBI

Linked Data

dbSNP Id: rs794726920
gnomAD v3: 14-28767473-C-CGCCGCCGCCGCCGCAGCAGCAGCA
gnomAD v4: 14-28767473-C-CGCCGCCGCCGCCGCAGCAGCAGCA
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.28767488_28767511dup , CM000676.2:g.28767488_28767511dup GRCh38
NC_000014.8:g.29236694_29236717dup , CM000676.1:g.29236694_29236717dup GRCh37
NC_000014.7:g.28306445_28306468dup NCBI36
NG_009367.1:g.5408_5431dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000706482.1:c.209_232dup ENSP00000516406.1:p.Pro77_Pro78insGlnGlnGlnGlnProProProPro
ENST00000313071.7:c.209_232dup MANE Select ENSP00000339004.3:p.Pro77_Pro78insGlnGlnGlnGlnProProProPro
ENST00000313071.6:c.209_232dup ENSP00000339004.3:p.Pro77_Pro78insGlnGlnGlnGlnProProProPro
NM_005249.4:c.209_232dup NP_005240.3:p.Pro77_Pro78insGlnGlnGlnGlnProProProPro
NM_005249.5:c.209_232dup MANE Select NP_005240.3:p.Pro77_Pro78insGlnGlnGlnGlnProProProPro
Search 100 bp 5'
Search 100 bp 3'