Canonical Allele Identifier: CA2624398549
Gene: FOXG1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.28767506_28767507insTA , CM000676.2:g.28767506_28767507insTA GRCh38
NC_000014.8:g.29236712_29236713insTA , CM000676.1:g.29236712_29236713insTA GRCh37
NC_000014.7:g.28306463_28306464insTA NCBI36
NG_009367.1:g.5426_5427insTA

Transcript Alleles

HGVS Amino-acid Change
ENST00000706482.1:c.227_228insTA ENSP00000516406.1:p.Pro77SerfsTer?
ENST00000313071.7:c.227_228insTA MANE Select ENSP00000339004.3:p.Pro77SerfsTer?
ENST00000313071.6:c.227_228insTA ENSP00000339004.3:p.Pro77SerfsTer?
NM_005249.4:c.227_228insTA NP_005240.3:p.Pro77SerfsTer?
NM_005249.5:c.227_228insTA MANE Select NP_005240.3:p.Pro77SerfsTer?