Canonical Allele Identifier: CA2125998669
Gene: FOXG1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.28767417_28767432delinsGCACCACCACCACCAC , CM000676.2:g.28767417_28767432delinsGCACCACCACCACCAC GRCh38
NC_000014.8:g.29236623_29236638delinsGCACCACCACCACCAC , CM000676.1:g.29236623_29236638delinsGCACCACCACCACCAC GRCh37
NC_000014.7:g.28306374_28306389delinsGCACCACCACCACCAC NCBI36
NG_009367.1:g.5337_5352delinsGCACCACCACCACCAC

Transcript Alleles

HGVS Amino-acid Change
ENST00000706482.1:c.138_153delinsGCACCACCACCACCAC ENSP00000516406.1:p.Gln46=
ENST00000313071.7:c.138_153delinsGCACCACCACCACCAC MANE Select ENSP00000339004.3:p.Gln46=
ENST00000313071.6:c.138_153delinsGCACCACCACCACCAC ENSP00000339004.3:p.Gln46=
NM_005249.4:c.138_153delinsGCACCACCACCACCAC NP_005240.3:p.Gln46=
NM_005249.5:c.138_153delinsGCACCACCACCACCAC MANE Select NP_005240.3:p.Gln46=
Search 100 bp 5'
Search 100 bp 3'