Canonical Allele Identifier: CA389476469
Gene: FOXG1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.28768346T>A , CM000676.2:g.28768346T>A GRCh38
NC_000014.8:g.29237552T>A , CM000676.1:g.29237552T>A GRCh37
NC_000014.7:g.28307303T>A NCBI36
NG_009367.1:g.6266T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000706482.1:c.1067T>A ENSP00000516406.1:p.Phe356Tyr
ENST00000313071.7:c.1067T>A MANE Select ENSP00000339004.3:p.Phe356Tyr
ENST00000313071.6:c.1067T>A ENSP00000339004.3:p.Phe356Tyr
NM_005249.4:c.1067T>A NP_005240.3:p.Phe356Tyr
NM_005249.5:c.1067T>A MANE Select NP_005240.3:p.Phe356Tyr