Canonical Allele Identifier: CA2126000379
Gene: FOXG1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.28768343_28768346delinsCCTT , CM000676.2:g.28768343_28768346delinsCCTT GRCh38
NC_000014.8:g.29237549_29237552delinsCCTT , CM000676.1:g.29237549_29237552delinsCCTT GRCh37
NC_000014.7:g.28307300_28307303delinsCCTT NCBI36
NG_009367.1:g.6263_6266delinsCCTT

Transcript Alleles

HGVS Amino-acid change
ENST00000706482.1:c.1064_1067delinsCCTT ENSP00000516406.1:p.Ser355=
ENST00000313071.7:c.1064_1067delinsCCTT MANE Select ENSP00000339004.3:p.Ser355=
ENST00000313071.6:c.1064_1067delinsCCTT ENSP00000339004.3:p.Ser355=
NM_005249.4:c.1064_1067delinsCCTT NP_005240.3:p.Ser355=
NM_005249.5:c.1064_1067delinsCCTT MANE Select NP_005240.3:p.Ser355=