Canonical Allele Identifier: CA2801003415
Gene: FOXG1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.28768413_28768414insACACCCAA , CM000676.2:g.28768413_28768414insACACCCAA GRCh38
NC_000014.8:g.29237619_29237620insACACCCAA , CM000676.1:g.29237619_29237620insACACCCAA GRCh37
NC_000014.7:g.28307370_28307371insACACCCAA NCBI36
NG_009367.1:g.6333_6334insACACCCAA

Transcript Alleles

HGVS Amino-acid Change
ENST00000706482.1:c.1134_1135insACACCCAA ENSP00000516406.1:p.Leu379ThrfsTer9
ENST00000313071.7:c.1134_1135insACACCCAA MANE Select ENSP00000339004.3:p.Leu379ThrfsTer9
ENST00000313071.6:c.1134_1135insACACCCAA ENSP00000339004.3:p.Leu379ThrfsTer9
NM_005249.4:c.1134_1135insACACCCAA NP_005240.3:p.Leu379ThrfsTer9
NM_005249.5:c.1134_1135insACACCCAA MANE Select NP_005240.3:p.Leu379ThrfsTer9