Canonical Allele Identifier: CA2580088020

Gene: FOXG1

Linked Data

• ClinVar Variation Id: 1704278
• ClinVar RCV Id: RCV002281625

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.28768120del , CM000676.2:g.28768120del	GRCh38
NC_000014.8:g.29237326del , CM000676.1:g.29237326del	GRCh37
NC_000014.7:g.28307077del	NCBI36
NG_009367.1:g.6040del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000706482.1:c.841del	ENSP00000516406.1:p.Arg281GlyfsTer?
ENST00000313071.7:c.841del MANE Select	ENSP00000339004.3:p.Arg281GlyfsTer?
ENST00000313071.6:c.841del	ENSP00000339004.3:p.Arg281GlyfsTer?
NM_005249.4:c.841del	NP_005240.3:p.Arg281GlyfsTer?
NM_005249.5:c.841del MANE Select	NP_005240.3:p.Arg281GlyfsTer?