Canonical Allele Identifier: CA2126000562
Gene: FOXG1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.28768841_28768843delinsGCC , CM000676.2:g.28768841_28768843delinsGCC GRCh38
NC_000014.8:g.29238047_29238049delinsGCC , CM000676.1:g.29238047_29238049delinsGCC GRCh37
NC_000014.7:g.28307798_28307800delinsGCC NCBI36
NG_009367.1:g.6761_6763delinsGCC

Transcript Alleles

HGVS Amino-acid Change
ENST00000706482.1:c.*92_*94delinsGCC ENSP00000516406.1:n.*92_*94delinsGCC
ENST00000313071.7:c.*92_*94delinsGCC MANE Select ENSP00000339004.3:n.*92_*94delinsGCC
ENST00000313071.6:c.*92_*94delinsGCC ENSP00000339004.3:n.*92_*94delinsGCC
NM_005249.4:c.*92_*94delinsGCC NP_005240.3:n.*92_*94delinsGCC
NM_005249.5:c.*92_*94delinsGCC MANE Select NP_005240.3:n.*92_*94delinsGCC