Canonical Allele Identifier: CA613324878

Gene: FOXG1

Linked Data

• dbSNP Id: rs1479330954
• gnomAD v2: 14-29237969-A-AT
• gnomAD v4: 14-28768763-A-AT
• MyVariant Identifiers: chr14:g.29237969_29237970insT (hg19) ; chr14:g.28768763_28768764insT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.28768763_28768764insT , CM000676.2:g.28768763_28768764insT	GRCh38
NC_000014.8:g.29237969_29237970insT , CM000676.1:g.29237969_29237970insT	GRCh37
NC_000014.7:g.28307720_28307721insT	NCBI36
NG_009367.1:g.6683_6684insT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000706482.1:c.*14_*15insT	ENSP00000516406.1:n.*14_*15insT
ENST00000313071.7:c.*14_*15insT MANE Select	ENSP00000339004.3:n.*14_*15insT
ENST00000313071.6:c.*14_*15insT	ENSP00000339004.3:n.*14_*15insT
NM_005249.4:c.*14_*15insT	NP_005240.3:n.*14_*15insT
NM_005249.5:c.*14_*15insT MANE Select	NP_005240.3:n.*14_*15insT