Canonical Allele Identifier: CA2126000065
Gene: FOXG1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.28767996C= , CM000676.2:g.28767996C= GRCh38
NC_000014.8:g.29237202C= , CM000676.1:g.29237202C= GRCh37
NC_000014.7:g.28306953C= NCBI36
NG_009367.1:g.5916C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000706482.1:c.717C= ENSP00000516406.1:p.Phe239=
ENST00000313071.7:c.717C= MANE Select ENSP00000339004.3:p.Phe239=
ENST00000313071.6:c.717C= ENSP00000339004.3:p.Phe239=
NM_005249.4:c.717C= NP_005240.3:p.Phe239=
NM_005249.5:c.717C= MANE Select NP_005240.3:p.Phe239=
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