Canonical Allele Identifier: CA704761543

Gene: FOXG1

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.28767483_28767515del , CM000676.2:g.28767483_28767515del	GRCh38
NC_000014.8:g.29236689_29236721del , CM000676.1:g.29236689_29236721del	GRCh37
NC_000014.7:g.28306440_28306472del	NCBI36
NG_009367.1:g.5403_5435del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000706482.1:c.204_236del	ENSP00000516406.1:p.Pro69_Pro79del
ENST00000313071.7:c.204_236del MANE Select	ENSP00000339004.3:p.Pro69_Pro79del
ENST00000313071.6:c.204_236del	ENSP00000339004.3:p.Pro69_Pro79del
NM_005249.4:c.204_236del	NP_005240.3:p.Pro69_Pro79del
NM_005249.5:c.204_236del MANE Select	NP_005240.3:p.Pro69_Pro79del