Canonical Allele Identifier: CA613324864
Gene: FOXG1 HGNC NCBI

Linked Data

dbSNP Id: rs1421580370
gnomAD v2: 14-29236787-AGCT-A
gnomAD v4: 14-28767581-AGCT-A
MyVariant Identifiers: chr14:g.29236788_29236790del (hg19) chr14:g.28767582_28767584del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.28767588_28767590del , CM000676.2:g.28767588_28767590del GRCh38
NC_000014.8:g.29236794_29236796del , CM000676.1:g.29236794_29236796del GRCh37
NC_000014.7:g.28306545_28306547del NCBI36
NG_009367.1:g.5508_5510del

Transcript Alleles

HGVS Amino-acid Change
ENST00000706482.1:c.309_311del ENSP00000516406.1:p.Leu104del
ENST00000313071.7:c.309_311del MANE Select ENSP00000339004.3:p.Leu104del
ENST00000313071.6:c.309_311del ENSP00000339004.3:p.Leu104del
NM_005249.4:c.309_311del NP_005240.3:p.Leu104del
NM_005249.5:c.309_311del MANE Select NP_005240.3:p.Leu104del
Search 100 bp 5'
Search 100 bp 3'