Canonical Allele Identifier: CA2125998944
Gene: FOXG1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.28767538_28767554delinsACGCGGGGCGCCCCGGC , CM000676.2:g.28767538_28767554delinsACGCGGGGCGCCCCGGC GRCh38
NC_000014.8:g.29236744_29236760delinsACGCGGGGCGCCCCGGC , CM000676.1:g.29236744_29236760delinsACGCGGGGCGCCCCGGC GRCh37
NC_000014.7:g.28306495_28306511delinsACGCGGGGCGCCCCGGC NCBI36
NG_009367.1:g.5458_5474delinsACGCGGGGCGCCCCGGC

Transcript Alleles

HGVS Amino-acid Change
ENST00000706482.1:c.259_275delinsACGCGGGGCGCCCCGGC ENSP00000516406.1:p.Thr87=
ENST00000313071.7:c.259_275delinsACGCGGGGCGCCCCGGC MANE Select ENSP00000339004.3:p.Thr87=
ENST00000313071.6:c.259_275delinsACGCGGGGCGCCCCGGC ENSP00000339004.3:p.Thr87=
NM_005249.4:c.259_275delinsACGCGGGGCGCCCCGGC NP_005240.3:p.Thr87=
NM_005249.5:c.259_275delinsACGCGGGGCGCCCCGGC MANE Select NP_005240.3:p.Thr87=
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Search 100 bp 3'