Canonical Allele Identifier: CA2125998747
Gene: FOXG1 HGNC NCBI

Linked Data

dbSNP Id: rs1881778895
gnomAD v4: 14-28767432-CCACCACCAT-C
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.28767441_28767449del , CM000676.2:g.28767441_28767449del GRCh38
NC_000014.8:g.29236647_29236655del , CM000676.1:g.29236647_29236655del GRCh37
NC_000014.7:g.28306398_28306406del NCBI36
NG_009367.1:g.5361_5369del

Transcript Alleles

HGVS Amino-acid Change
ENST00000706482.1:c.162_170del ENSP00000516406.1:p.His55_His57del
ENST00000313071.7:c.162_170del MANE Select ENSP00000339004.3:p.His55_His57del
ENST00000313071.6:c.162_170del ENSP00000339004.3:p.His55_His57del
NM_005249.4:c.162_170del NP_005240.3:p.His55_His57del
NM_005249.5:c.162_170del MANE Select NP_005240.3:p.His55_His57del
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