Canonical Allele Identifier: CA2830782519
Gene: FOXG1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.28767564del , CM000676.2:g.28767564del GRCh38
NC_000014.8:g.29236770del , CM000676.1:g.29236770del GRCh37
NC_000014.7:g.28306521del NCBI36
NG_009367.1:g.5484del

Transcript Alleles

HGVS Amino-acid Change
ENST00000706482.1:c.285del ENSP00000516406.1:p.Asp95GlufsTer?
ENST00000313071.7:c.285del MANE Select ENSP00000339004.3:p.Asp95GlufsTer?
ENST00000313071.6:c.285del ENSP00000339004.3:p.Asp95GlufsTer?
NM_005249.4:c.285del NP_005240.3:p.Asp95GlufsTer?
NM_005249.5:c.285del MANE Select NP_005240.3:p.Asp95GlufsTer?