Canonical Allele Identifier: CA2624398506
Gene: FOXG1 HGNC NCBI

Linked Data

gnomAD v4: 14-28767462-CGCCCCGCAACCGCCGCCGCCGCCG-C
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.28767463_28767486del , CM000676.2:g.28767463_28767486del GRCh38
NC_000014.8:g.29236669_29236692del , CM000676.1:g.29236669_29236692del GRCh37
NC_000014.7:g.28306420_28306443del NCBI36
NG_009367.1:g.5383_5406del

Transcript Alleles

HGVS Amino-acid Change
ENST00000706482.1:c.184_207del ENSP00000516406.1:p.Ala62_Pro69del
ENST00000313071.7:c.184_207del MANE Select ENSP00000339004.3:p.Ala62_Pro69del
ENST00000313071.6:c.184_207del ENSP00000339004.3:p.Ala62_Pro69del
NM_005249.4:c.184_207del NP_005240.3:p.Ala62_Pro69del
NM_005249.5:c.184_207del MANE Select NP_005240.3:p.Ala62_Pro69del
Search 100 bp 5'
Search 100 bp 3'