Canonical Allele Identifier: CA486098237

Gene: FOXG1

Linked Data

• gnomAD v4: 14-28767603-A-T
• MyVariant Identifiers: chr14:g.29236809A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.28767603A>T , CM000676.2:g.28767603A>T	GRCh38
NC_000014.8:g.29236809A>T , CM000676.1:g.29236809A>T	GRCh37
NC_000014.7:g.28306560A>T	NCBI36
NG_009367.1:g.5523A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000706482.1:c.324A>T	ENSP00000516406.1:p.Pro108=
ENST00000313071.7:c.324A>T MANE Select	ENSP00000339004.3:p.Pro108=
ENST00000313071.6:c.324A>T	ENSP00000339004.3:p.Pro108=
NM_005249.4:c.324A>T	NP_005240.3:p.Pro108=
NM_005249.5:c.324A>T MANE Select	NP_005240.3:p.Pro108=