Canonical Allele Identifier: CA2801003469

Gene: FOXG1

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.28768810_28768811insG , CM000676.2:g.28768810_28768811insG	GRCh38
NC_000014.8:g.29238016_29238017insG , CM000676.1:g.29238016_29238017insG	GRCh37
NC_000014.7:g.28307767_28307768insG	NCBI36
NG_009367.1:g.6730_6731insG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000706482.1:c.*61_*62insG	ENSP00000516406.1:n.*61_*62insG
ENST00000313071.7:c.*61_*62insG MANE Select	ENSP00000339004.3:n.*61_*62insG
ENST00000313071.6:c.*61_*62insG	ENSP00000339004.3:n.*61_*62insG
NM_005249.4:c.*61_*62insG	NP_005240.3:n.*61_*62insG
NM_005249.5:c.*61_*62insG MANE Select	NP_005240.3:n.*61_*62insG