Canonical Allele Identifier: CA2125999546
Gene: FOXG1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.28767747G= , CM000676.2:g.28767747G= GRCh38
NC_000014.8:g.29236953G= , CM000676.1:g.29236953G= GRCh37
NC_000014.7:g.28306704G= NCBI36
NG_009367.1:g.5667G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000706482.1:c.468G= ENSP00000516406.1:p.Lys156=
ENST00000313071.7:c.468G= MANE Select ENSP00000339004.3:p.Lys156=
ENST00000313071.6:c.468G= ENSP00000339004.3:p.Lys156=
NM_005249.4:c.468G= NP_005240.3:p.Lys156=
NM_005249.5:c.468G= MANE Select NP_005240.3:p.Lys156=