Canonical Allele Identifier: CA2126000575
Gene: FOXG1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.28768849_28768850delinsCT , CM000676.2:g.28768849_28768850delinsCT GRCh38
NC_000014.8:g.29238055_29238056delinsCT , CM000676.1:g.29238055_29238056delinsCT GRCh37
NC_000014.7:g.28307806_28307807delinsCT NCBI36
NG_009367.1:g.6769_6770delinsCT

Transcript Alleles

HGVS Amino-acid Change
ENST00000706482.1:c.*100_*101delinsCT ENSP00000516406.1:n.*100_*101delinsCT
ENST00000313071.7:c.*100_*101delinsCT MANE Select ENSP00000339004.3:n.*100_*101delinsCT
ENST00000313071.6:c.*100_*101delinsCT ENSP00000339004.3:n.*100_*101delinsCT
NM_005249.4:c.*100_*101delinsCT NP_005240.3:n.*100_*101delinsCT
NM_005249.5:c.*100_*101delinsCT MANE Select NP_005240.3:n.*100_*101delinsCT