Canonical Allele Identifier: CA2575498212
Gene: FOXG1 HGNC NCBI

Linked Data

gnomAD v4: 14-28767594-GCCGCCGCCA-G
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.28767600_28767608del , CM000676.2:g.28767600_28767608del GRCh38
NC_000014.8:g.29236806_29236814del , CM000676.1:g.29236806_29236814del GRCh37
NC_000014.7:g.28306557_28306565del NCBI36
NG_009367.1:g.5520_5528del

Transcript Alleles

HGVS Amino-acid Change
ENST00000706482.1:c.321_329del ENSP00000516406.1:p.Pro108_Pro110del
ENST00000313071.7:c.321_329del MANE Select ENSP00000339004.3:p.Pro108_Pro110del
ENST00000313071.6:c.321_329del ENSP00000339004.3:p.Pro108_Pro110del
NM_005249.4:c.321_329del NP_005240.3:p.Pro108_Pro110del
NM_005249.5:c.321_329del MANE Select NP_005240.3:p.Pro108_Pro110del
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