Canonical Allele Identifier: CA2997007777
Gene: FOXG1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.28767516_28767527del , CM000676.2:g.28767516_28767527del GRCh38
NC_000014.8:g.29236722_29236733del , CM000676.1:g.29236722_29236733del GRCh37
NC_000014.7:g.28306473_28306484del NCBI36
NG_009367.1:g.5436_5447del

Transcript Alleles

HGVS Amino-acid Change
ENST00000706482.1:c.237_248del ENSP00000516406.1:p.Pro80_Gln83del
ENST00000313071.7:c.237_248del MANE Select ENSP00000339004.3:p.Pro80_Gln83del
ENST00000313071.6:c.237_248del ENSP00000339004.3:p.Pro80_Gln83del
NM_005249.4:c.237_248del NP_005240.3:p.Pro80_Gln83del
NM_005249.5:c.237_248del MANE Select NP_005240.3:p.Pro80_Gln83del