Canonical Allele Identifier: CA2801003478
Gene: FOXG1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.28768857dup , CM000676.2:g.28768857dup GRCh38
NC_000014.8:g.29238063dup , CM000676.1:g.29238063dup GRCh37
NC_000014.7:g.28307814dup NCBI36
NG_009367.1:g.6777dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000706482.1:c.*108dup ENSP00000516406.1:n.*108dup
ENST00000313071.7:c.*108dup MANE Select ENSP00000339004.3:n.*108dup
ENST00000313071.6:c.*108dup ENSP00000339004.3:n.*108dup
NM_005249.4:c.*108dup NP_005240.3:n.*108dup
NM_005249.5:c.*108dup MANE Select NP_005240.3:n.*108dup