Canonical Allele Identifier: CA2125999009
Gene: FOXG1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.28767557_28767560delinsCCGA , CM000676.2:g.28767557_28767560delinsCCGA GRCh38
NC_000014.8:g.29236763_29236766delinsCCGA , CM000676.1:g.29236763_29236766delinsCCGA GRCh37
NC_000014.7:g.28306514_28306517delinsCCGA NCBI36
NG_009367.1:g.5477_5480delinsCCGA

Transcript Alleles

HGVS Amino-acid Change
ENST00000706482.1:c.278_281delinsCCGA ENSP00000516406.1:p.Ala93=
ENST00000313071.7:c.278_281delinsCCGA MANE Select ENSP00000339004.3:p.Ala93=
ENST00000313071.6:c.278_281delinsCCGA ENSP00000339004.3:p.Ala93=
NM_005249.4:c.278_281delinsCCGA NP_005240.3:p.Ala93=
NM_005249.5:c.278_281delinsCCGA MANE Select NP_005240.3:p.Ala93=
Search 100 bp 5'
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