Canonical Allele Identifier: CA486098070
Gene: FOXG1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.28767504_28767505del , CM000676.2:g.28767504_28767505del GRCh38
NC_000014.8:g.29236710_29236711del , CM000676.1:g.29236710_29236711del GRCh37
NC_000014.7:g.28306461_28306462del NCBI36
NG_009367.1:g.5424_5425del

Transcript Alleles

HGVS Amino-acid Change
ENST00000706482.1:c.225_226del ENSP00000516406.1:p.Pro76AlafsTer?
ENST00000313071.7:c.225_226del MANE Select ENSP00000339004.3:p.Pro76AlafsTer?
ENST00000313071.6:c.225_226del ENSP00000339004.3:p.Pro76AlafsTer?
NM_005249.4:c.225_226del NP_005240.3:p.Pro76AlafsTer?
NM_005249.5:c.225_226del MANE Select NP_005240.3:p.Pro76AlafsTer?