Canonical Allele Identifier: CA2624398490
Gene: FOXG1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.28767439_28767440del , CM000676.2:g.28767439_28767440del GRCh38
NC_000014.8:g.29236645_29236646del , CM000676.1:g.29236645_29236646del GRCh37
NC_000014.7:g.28306396_28306397del NCBI36
NG_009367.1:g.5359_5360del

Transcript Alleles

HGVS Amino-acid Change
ENST00000706482.1:c.160_161del ENSP00000516406.1:p.His54SerfsTer?
ENST00000313071.7:c.160_161del MANE Select ENSP00000339004.3:p.His54SerfsTer?
ENST00000313071.6:c.160_161del ENSP00000339004.3:p.His54SerfsTer?
NM_005249.4:c.160_161del NP_005240.3:p.His54SerfsTer?
NM_005249.5:c.160_161del MANE Select NP_005240.3:p.His54SerfsTer?