Canonical Allele Identifier: CA2624398855
Gene: FOXG1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.28767603_28767624del , CM000676.2:g.28767603_28767624del GRCh38
NC_000014.8:g.29236809_29236830del , CM000676.1:g.29236809_29236830del GRCh37
NC_000014.7:g.28306560_28306581del NCBI36
NG_009367.1:g.5523_5544del

Transcript Alleles

HGVS Amino-acid Change
ENST00000706482.1:c.324_345del ENSP00000516406.1:p.Pro109TrpfsTer?
ENST00000313071.7:c.324_345del MANE Select ENSP00000339004.3:p.Pro109TrpfsTer?
ENST00000313071.6:c.324_345del ENSP00000339004.3:p.Pro109TrpfsTer?
NM_005249.4:c.324_345del NP_005240.3:p.Pro109TrpfsTer?
NM_005249.5:c.324_345del MANE Select NP_005240.3:p.Pro109TrpfsTer?