Canonical Allele Identifier: CA2125998877
Gene: FOXG1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.28767499_28767507delinsCCGCCGCCG , CM000676.2:g.28767499_28767507delinsCCGCCGCCG GRCh38
NC_000014.8:g.29236705_29236713delinsCCGCCGCCG , CM000676.1:g.29236705_29236713delinsCCGCCGCCG GRCh37
NC_000014.7:g.28306456_28306464delinsCCGCCGCCG NCBI36
NG_009367.1:g.5419_5427delinsCCGCCGCCG

Transcript Alleles

HGVS Amino-acid Change
ENST00000706482.1:c.220_228delinsCCGCCGCCG ENSP00000516406.1:p.Pro74=
ENST00000313071.7:c.220_228delinsCCGCCGCCG MANE Select ENSP00000339004.3:p.Pro74=
ENST00000313071.6:c.220_228delinsCCGCCGCCG ENSP00000339004.3:p.Pro74=
NM_005249.4:c.220_228delinsCCGCCGCCG NP_005240.3:p.Pro74=
NM_005249.5:c.220_228delinsCCGCCGCCG MANE Select NP_005240.3:p.Pro74=
Search 100 bp 5'
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