Canonical Allele Identifier: CA2695219197
Gene: FOXG1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.28768137dup , CM000676.2:g.28768137dup GRCh38
NC_000014.8:g.29237343dup , CM000676.1:g.29237343dup GRCh37
NC_000014.7:g.28307094dup NCBI36
NG_009367.1:g.6057dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000706482.1:c.858dup ENSP00000516406.1:p.Lys287GlnfsTer?
ENST00000313071.7:c.858dup MANE Select ENSP00000339004.3:p.Lys287GlnfsTer?
ENST00000313071.6:c.858dup ENSP00000339004.3:p.Lys287GlnfsTer?
NM_005249.4:c.858dup NP_005240.3:p.Lys287GlnfsTer?
NM_005249.5:c.858dup MANE Select NP_005240.3:p.Lys287GlnfsTer?