Canonical Allele Identifier: CA2695219191
Gene: FOXG1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.28767754del , CM000676.2:g.28767754del GRCh38
NC_000014.8:g.29236960del , CM000676.1:g.29236960del GRCh37
NC_000014.7:g.28306711del NCBI36
NG_009367.1:g.5674del

Transcript Alleles

HGVS Amino-acid change
ENST00000706482.1:c.475del ENSP00000516406.1:p.Ala159ArgfsTer?
ENST00000313071.7:c.475del MANE Select ENSP00000339004.3:p.Ala159ArgfsTer?
ENST00000313071.6:c.475del ENSP00000339004.3:p.Ala159ArgfsTer?
NM_005249.4:c.475del NP_005240.3:p.Ala159ArgfsTer?
NM_005249.5:c.475del MANE Select NP_005240.3:p.Ala159ArgfsTer?