Canonical Allele Identifier: CA2624398473
Gene: FOXG1 HGNC NCBI

Linked Data

gnomAD v4: 14-28767420-CCACCACCACCACCACCACCAT-C
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.28767431_28767451del , CM000676.2:g.28767431_28767451del GRCh38
NC_000014.8:g.29236637_29236657del , CM000676.1:g.29236637_29236657del GRCh37
NC_000014.7:g.28306388_28306408del NCBI36
NG_009367.1:g.5351_5371del

Transcript Alleles

HGVS Amino-acid Change
ENST00000706482.1:c.152_172del ENSP00000516406.1:p.His51_His57del
ENST00000313071.7:c.152_172del MANE Select ENSP00000339004.3:p.His51_His57del
ENST00000313071.6:c.152_172del ENSP00000339004.3:p.His51_His57del
NM_005249.4:c.152_172del NP_005240.3:p.His51_His57del
NM_005249.5:c.152_172del MANE Select NP_005240.3:p.His51_His57del
Search 100 bp 5'
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