Canonical Allele Identifier: CA2575498205
Gene: FOXG1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.28767544_28767545del , CM000676.2:g.28767544_28767545del GRCh38
NC_000014.8:g.29236750_29236751del , CM000676.1:g.29236750_29236751del GRCh37
NC_000014.7:g.28306501_28306502del NCBI36
NG_009367.1:g.5464_5465del

Transcript Alleles

HGVS Amino-acid Change
ENST00000706482.1:c.265_266del ENSP00000516406.1:p.Gly89ArgfsTer?
ENST00000313071.7:c.265_266del MANE Select ENSP00000339004.3:p.Gly89ArgfsTer?
ENST00000313071.6:c.265_266del ENSP00000339004.3:p.Gly89ArgfsTer?
NM_005249.4:c.265_266del NP_005240.3:p.Gly89ArgfsTer?
NM_005249.5:c.265_266del MANE Select NP_005240.3:p.Gly89ArgfsTer?