Canonical Allele Identifier: CA2624398922
Gene: FOXG1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.28767606del , CM000676.2:g.28767606del GRCh38
NC_000014.8:g.29236812del , CM000676.1:g.29236812del GRCh37
NC_000014.7:g.28306563del NCBI36
NG_009367.1:g.5526del

Transcript Alleles

HGVS Amino-acid change
ENST00000706482.1:c.327del ENSP00000516406.1:p.Pro110HisfsTer?
ENST00000313071.7:c.327del MANE Select ENSP00000339004.3:p.Pro110HisfsTer?
ENST00000313071.6:c.327del ENSP00000339004.3:p.Pro110HisfsTer?
NM_005249.4:c.327del NP_005240.3:p.Pro110HisfsTer?
NM_005249.5:c.327del MANE Select NP_005240.3:p.Pro110HisfsTer?