Canonical Allele Identifier: CA2125999432
Gene: FOXG1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.28767716A= , CM000676.2:g.28767716A= GRCh38
NC_000014.8:g.29236922A= , CM000676.1:g.29236922A= GRCh37
NC_000014.7:g.28306673A= NCBI36
NG_009367.1:g.5636A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000706482.1:c.437A= ENSP00000516406.1:p.Glu146=
ENST00000313071.7:c.437A= MANE Select ENSP00000339004.3:p.Glu146=
ENST00000313071.6:c.437A= ENSP00000339004.3:p.Glu146=
NM_005249.4:c.437A= NP_005240.3:p.Glu146=
NM_005249.5:c.437A= MANE Select NP_005240.3:p.Glu146=