Canonical Allele Identifier: CA2801003477
Gene: FOXG1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.28768849C>G , CM000676.2:g.28768849C>G GRCh38
NC_000014.8:g.29238055C>G , CM000676.1:g.29238055C>G GRCh37
NC_000014.7:g.28307806C>G NCBI36
NG_009367.1:g.6769C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000706482.1:c.*100C>G ENSP00000516406.1:n.*100C>G
ENST00000313071.7:c.*100C>G MANE Select ENSP00000339004.3:n.*100C>G
ENST00000313071.6:c.*100C>G ENSP00000339004.3:n.*100C>G
NM_005249.4:c.*100C>G NP_005240.3:n.*100C>G
NM_005249.5:c.*100C>G MANE Select NP_005240.3:n.*100C>G
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