Canonical Allele Identifier: CA2624399950
Gene: FOXG1 HGNC NCBI

Linked Data

gnomAD v4: 14-28768150-CGCCTCACCTCCACCG-C
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.28768160_28768174del , CM000676.2:g.28768160_28768174del GRCh38
NC_000014.8:g.29237366_29237380del , CM000676.1:g.29237366_29237380del GRCh37
NC_000014.7:g.28307117_28307131del NCBI36
NG_009367.1:g.6080_6094del

Transcript Alleles

HGVS Amino-acid Change
ENST00000706482.1:c.881_895del ENSP00000516406.1:p.Ser294_Thr298del
ENST00000313071.7:c.881_895del MANE Select ENSP00000339004.3:p.Ser294_Thr298del
ENST00000313071.6:c.881_895del ENSP00000339004.3:p.Ser294_Thr298del
NM_005249.4:c.881_895del NP_005240.3:p.Ser294_Thr298del
NM_005249.5:c.881_895del MANE Select NP_005240.3:p.Ser294_Thr298del
Search 100 bp 5'
Search 100 bp 3'