Canonical Allele Identifier: CA2126000574
Gene: FOXG1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.28768848_28768850delinsCCT , CM000676.2:g.28768848_28768850delinsCCT GRCh38
NC_000014.8:g.29238054_29238056delinsCCT , CM000676.1:g.29238054_29238056delinsCCT GRCh37
NC_000014.7:g.28307805_28307807delinsCCT NCBI36
NG_009367.1:g.6768_6770delinsCCT

Transcript Alleles

HGVS Amino-acid Change
ENST00000706482.1:c.*99_*101delinsCCT ENSP00000516406.1:n.*99_*101delinsCCT
ENST00000313071.7:c.*99_*101delinsCCT MANE Select ENSP00000339004.3:n.*99_*101delinsCCT
ENST00000313071.6:c.*99_*101delinsCCT ENSP00000339004.3:n.*99_*101delinsCCT
NM_005249.4:c.*99_*101delinsCCT NP_005240.3:n.*99_*101delinsCCT
NM_005249.5:c.*99_*101delinsCCT MANE Select NP_005240.3:n.*99_*101delinsCCT