Canonical Allele Identifier: CA2126000296
Gene: FOXG1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.28768132G= , CM000676.2:g.28768132G= GRCh38
NC_000014.8:g.29237338G= , CM000676.1:g.29237338G= GRCh37
NC_000014.7:g.28307089G= NCBI36
NG_009367.1:g.6052G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000706482.1:c.853G= ENSP00000516406.1:p.Ala285=
ENST00000313071.7:c.853G= MANE Select ENSP00000339004.3:p.Ala285=
ENST00000313071.6:c.853G= ENSP00000339004.3:p.Ala285=
NM_005249.4:c.853G= NP_005240.3:p.Ala285=
NM_005249.5:c.853G= MANE Select NP_005240.3:p.Ala285=
Search 100 bp 5'
Search 100 bp 3'