Canonical Allele Identifier: CA2125998812
Gene: FOXG1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.28767450_28767477delinsCCCGCCGCCGCCCGCCCCGCAACCGCCG , CM000676.2:g.28767450_28767477delinsCCCGCCGCCGCCCGCCCCGCAACCGCCG GRCh38
NC_000014.8:g.29236656_29236683delinsCCCGCCGCCGCCCGCCCCGCAACCGCCG , CM000676.1:g.29236656_29236683delinsCCCGCCGCCGCCCGCCCCGCAACCGCCG GRCh37
NC_000014.7:g.28306407_28306434delinsCCCGCCGCCGCCCGCCCCGCAACCGCCG NCBI36
NG_009367.1:g.5370_5397delinsCCCGCCGCCGCCCGCCCCGCAACCGCCG

Transcript Alleles

HGVS Amino-acid Change
ENST00000706482.1:c.171_198delinsCCCGCCGCCGCCCGCCCCGCAACCGCCG ENSP00000516406.1:p.His57=
ENST00000313071.7:c.171_198delinsCCCGCCGCCGCCCGCCCCGCAACCGCCG MANE Select ENSP00000339004.3:p.His57=
ENST00000313071.6:c.171_198delinsCCCGCCGCCGCCCGCCCCGCAACCGCCG ENSP00000339004.3:p.His57=
NM_005249.4:c.171_198delinsCCCGCCGCCGCCCGCCCCGCAACCGCCG NP_005240.3:p.His57=
NM_005249.5:c.171_198delinsCCCGCCGCCGCCCGCCCCGCAACCGCCG MANE Select NP_005240.3:p.His57=