Canonical Allele Identifier: CA2624398509
Gene: FOXG1 HGNC NCBI

Linked Data

gnomAD v4: 14-28767465-CCCGCAACCGCCGCCGCCG-C
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.28767471_28767488del , CM000676.2:g.28767471_28767488del GRCh38
NC_000014.8:g.29236677_29236694del , CM000676.1:g.29236677_29236694del GRCh37
NC_000014.7:g.28306428_28306445del NCBI36
NG_009367.1:g.5391_5408del

Transcript Alleles

HGVS Amino-acid Change
ENST00000706482.1:c.192_209del ENSP00000516406.1:p.Pro65_Gln70del
ENST00000313071.7:c.192_209del MANE Select ENSP00000339004.3:p.Pro65_Gln70del
ENST00000313071.6:c.192_209del ENSP00000339004.3:p.Pro65_Gln70del
NM_005249.4:c.192_209del NP_005240.3:p.Pro65_Gln70del
NM_005249.5:c.192_209del MANE Select NP_005240.3:p.Pro65_Gln70del
Search 100 bp 5'
Search 100 bp 3'