Canonical Allele Identifier: CA2125998901
Gene: FOXG1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.28767528_28767529delinsGC , CM000676.2:g.28767528_28767529delinsGC GRCh38
NC_000014.8:g.29236734_29236735delinsGC , CM000676.1:g.29236734_29236735delinsGC GRCh37
NC_000014.7:g.28306485_28306486delinsGC NCBI36
NG_009367.1:g.5448_5449delinsGC

Transcript Alleles

HGVS Amino-acid Change
ENST00000706482.1:c.249_250delinsGC ENSP00000516406.1:p.Gln83=
ENST00000313071.7:c.249_250delinsGC MANE Select ENSP00000339004.3:p.Gln83=
ENST00000313071.6:c.249_250delinsGC ENSP00000339004.3:p.Gln83=
NM_005249.4:c.249_250delinsGC NP_005240.3:p.Gln83=
NM_005249.5:c.249_250delinsGC MANE Select NP_005240.3:p.Gln83=