Canonical Allele Identifier: CA2624399051
Gene: FOXG1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.28767662_28767772del , CM000676.2:g.28767662_28767772del GRCh38
NC_000014.8:g.29236868_29236978del , CM000676.1:g.29236868_29236978del GRCh37
NC_000014.7:g.28306619_28306729del NCBI36
NG_009367.1:g.5582_5692del

Transcript Alleles

HGVS Amino-acid Change
ENST00000706482.1:c.383_493del ENSP00000516406.1:p.Gly128_Lys164del
ENST00000313071.7:c.383_493del MANE Select ENSP00000339004.3:p.Gly128_Lys164del
ENST00000313071.6:c.383_493del ENSP00000339004.3:p.Gly128_Lys164del
NM_005249.4:c.383_493del NP_005240.3:p.Gly128_Lys164del
NM_005249.5:c.383_493del MANE Select NP_005240.3:p.Gly128_Lys164del