Canonical Allele Identifier: CA2126000078
Gene: FOXG1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.28768007C= , CM000676.2:g.28768007C= GRCh38
NC_000014.8:g.29237213C= , CM000676.1:g.29237213C= GRCh37
NC_000014.7:g.28306964C= NCBI36
NG_009367.1:g.5927C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000706482.1:c.728C= ENSP00000516406.1:p.Pro243=
ENST00000313071.7:c.728C= MANE Select ENSP00000339004.3:p.Pro243=
ENST00000313071.6:c.728C= ENSP00000339004.3:p.Pro243=
NM_005249.4:c.728C= NP_005240.3:p.Pro243=
NM_005249.5:c.728C= MANE Select NP_005240.3:p.Pro243=