Canonical Allele Identifier: CA2624398994
Gene: FOXG1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.28767634_28767648del , CM000676.2:g.28767634_28767648del GRCh38
NC_000014.8:g.29236840_29236854del , CM000676.1:g.29236840_29236854del GRCh37
NC_000014.7:g.28306591_28306605del NCBI36
NG_009367.1:g.5554_5568del

Transcript Alleles

HGVS Amino-acid Change
ENST00000706482.1:c.355_369del ENSP00000516406.1:p.Ala119_Gly123del
ENST00000313071.7:c.355_369del MANE Select ENSP00000339004.3:p.Ala119_Gly123del
ENST00000313071.6:c.355_369del ENSP00000339004.3:p.Ala119_Gly123del
NM_005249.4:c.355_369del NP_005240.3:p.Ala119_Gly123del
NM_005249.5:c.355_369del MANE Select NP_005240.3:p.Ala119_Gly123del