Canonical Allele Identifier: CA2126000128

Gene: FOXG1

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.28768028G= , CM000676.2:g.28768028G=	GRCh38
NC_000014.8:g.29237234G= , CM000676.1:g.29237234G=	GRCh37
NC_000014.7:g.28306985G=	NCBI36
NG_009367.1:g.5948G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000706482.1:c.749G=	ENSP00000516406.1:p.Gly250=
ENST00000313071.7:c.749G= MANE Select	ENSP00000339004.3:p.Gly250=
ENST00000313071.6:c.749G=	ENSP00000339004.3:p.Gly250=
NM_005249.4:c.749G=	NP_005240.3:p.Gly250=
NM_005249.5:c.749G= MANE Select	NP_005240.3:p.Gly250=