Canonical Allele Identifier: CA2125999100
Gene: FOXG1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.28767592_28767597delinsCCGCCG , CM000676.2:g.28767592_28767597delinsCCGCCG GRCh38
NC_000014.8:g.29236798_29236803delinsCCGCCG , CM000676.1:g.29236798_29236803delinsCCGCCG GRCh37
NC_000014.7:g.28306549_28306554delinsCCGCCG NCBI36
NG_009367.1:g.5512_5517delinsCCGCCG

Transcript Alleles

HGVS Amino-acid Change
ENST00000706482.1:c.313_318delinsCCGCCG ENSP00000516406.1:p.Pro105=
ENST00000313071.7:c.313_318delinsCCGCCG MANE Select ENSP00000339004.3:p.Pro105=
ENST00000313071.6:c.313_318delinsCCGCCG ENSP00000339004.3:p.Pro105=
NM_005249.4:c.313_318delinsCCGCCG NP_005240.3:p.Pro105=
NM_005249.5:c.313_318delinsCCGCCG MANE Select NP_005240.3:p.Pro105=