Canonical Allele Identifier: CA2580087986
Gene: FOXG1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.28767413_28767439del , CM000676.2:g.28767413_28767439del GRCh38
NC_000014.8:g.29236619_29236645del , CM000676.1:g.29236619_29236645del GRCh37
NC_000014.7:g.28306370_28306396del NCBI36
NG_009367.1:g.5333_5359del

Transcript Alleles

HGVS Amino-acid Change
ENST00000706482.1:c.134_160del ENSP00000516406.1:p.Pro45_His53del
ENST00000313071.7:c.134_160del MANE Select ENSP00000339004.3:p.Pro45_His53del
ENST00000313071.6:c.134_160del ENSP00000339004.3:p.Pro45_His53del
NM_005249.4:c.134_160del NP_005240.3:p.Pro45_His53del
NM_005249.5:c.134_160del MANE Select NP_005240.3:p.Pro45_His53del