Canonical Allele Identifier: CA2125998874
Gene: FOXG1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.28767497_28767506delinsAGCCGCCGCC , CM000676.2:g.28767497_28767506delinsAGCCGCCGCC GRCh38
NC_000014.8:g.29236703_29236712delinsAGCCGCCGCC , CM000676.1:g.29236703_29236712delinsAGCCGCCGCC GRCh37
NC_000014.7:g.28306454_28306463delinsAGCCGCCGCC NCBI36
NG_009367.1:g.5417_5426delinsAGCCGCCGCC

Transcript Alleles

HGVS Amino-acid Change
ENST00000706482.1:c.218_227delinsAGCCGCCGCC ENSP00000516406.1:p.Gln73=
ENST00000313071.7:c.218_227delinsAGCCGCCGCC MANE Select ENSP00000339004.3:p.Gln73=
ENST00000313071.6:c.218_227delinsAGCCGCCGCC ENSP00000339004.3:p.Gln73=
NM_005249.4:c.218_227delinsAGCCGCCGCC NP_005240.3:p.Gln73=
NM_005249.5:c.218_227delinsAGCCGCCGCC MANE Select NP_005240.3:p.Gln73=