Canonical Allele Identifier: CA2801003336
Gene: FOXG1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.28767989_28767990insCACCAAACACACCCAACACA , CM000676.2:g.28767989_28767990insCACCAAACACACCCAACACA GRCh38
NC_000014.8:g.29237195_29237196insCACCAAACACACCCAACACA , CM000676.1:g.29237195_29237196insCACCAAACACACCCAACACA GRCh37
NC_000014.7:g.28306946_28306947insCACCAAACACACCCAACACA NCBI36
NG_009367.1:g.5909_5910insCACCAAACACACCCAACACA

Transcript Alleles

HGVS Amino-acid Change
ENST00000706482.1:c.710_711insCACCAAACACACCCAACACA ENSP00000516406.1:p.Lys237AsnfsTer11
ENST00000313071.7:c.710_711insCACCAAACACACCCAACACA MANE Select ENSP00000339004.3:p.Lys237AsnfsTer11
ENST00000313071.6:c.710_711insCACCAAACACACCCAACACA ENSP00000339004.3:p.Lys237AsnfsTer11
NM_005249.4:c.710_711insCACCAAACACACCCAACACA NP_005240.3:p.Lys237AsnfsTer11
NM_005249.5:c.710_711insCACCAAACACACCCAACACA MANE Select NP_005240.3:p.Lys237AsnfsTer11