Canonical Allele Identifier: CA2125998764
Gene: FOXG1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.28767438_28767441delinsCCAT , CM000676.2:g.28767438_28767441delinsCCAT GRCh38
NC_000014.8:g.29236644_29236647delinsCCAT , CM000676.1:g.29236644_29236647delinsCCAT GRCh37
NC_000014.7:g.28306395_28306398delinsCCAT NCBI36
NG_009367.1:g.5358_5361delinsCCAT

Transcript Alleles

HGVS Amino-acid Change
ENST00000706482.1:c.159_162delinsCCAT ENSP00000516406.1:p.His53=
ENST00000313071.7:c.159_162delinsCCAT MANE Select ENSP00000339004.3:p.His53=
ENST00000313071.6:c.159_162delinsCCAT ENSP00000339004.3:p.His53=
NM_005249.4:c.159_162delinsCCAT NP_005240.3:p.His53=
NM_005249.5:c.159_162delinsCCAT MANE Select NP_005240.3:p.His53=
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