Canonical Allele Identifier: CA2695219192
Gene: FOXG1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.28767758_28767767del , CM000676.2:g.28767758_28767767del GRCh38
NC_000014.8:g.29236964_29236973del , CM000676.1:g.29236964_29236973del GRCh37
NC_000014.7:g.28306715_28306724del NCBI36
NG_009367.1:g.5678_5687del

Transcript Alleles

HGVS Amino-acid Change
ENST00000706482.1:c.479_488del ENSP00000516406.1:p.Gly160AlafsTer29
ENST00000313071.7:c.479_488del MANE Select ENSP00000339004.3:p.Gly160AlafsTer29
ENST00000313071.6:c.479_488del ENSP00000339004.3:p.Gly160AlafsTer29
NM_005249.4:c.479_488del NP_005240.3:p.Gly160AlafsTer29
NM_005249.5:c.479_488del MANE Select NP_005240.3:p.Gly160AlafsTer29
Search 100 bp 5'
Search 100 bp 3'