Canonical Allele Identifier: CA2624398778
Gene: FOXG1 HGNC NCBI

Linked Data

gnomAD v4: 14-28767553-GCC-G
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.28767554_28767555del , CM000676.2:g.28767554_28767555del GRCh38
NC_000014.8:g.29236760_29236761del , CM000676.1:g.29236760_29236761del GRCh37
NC_000014.7:g.28306511_28306512del NCBI36
NG_009367.1:g.5474_5475del

Transcript Alleles

HGVS Amino-acid Change
ENST00000706482.1:c.275_276del ENSP00000516406.1:p.Ala92GlyfsTer28
ENST00000313071.7:c.275_276del MANE Select ENSP00000339004.3:p.Ala92GlyfsTer28
ENST00000313071.6:c.275_276del ENSP00000339004.3:p.Ala92GlyfsTer28
NM_005249.4:c.275_276del NP_005240.3:p.Ala92GlyfsTer28
NM_005249.5:c.275_276del MANE Select NP_005240.3:p.Ala92GlyfsTer28
Search 100 bp 5'
Search 100 bp 3'