Canonical Allele Identifier: CA2624400709
Gene: FOXG1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.28768809_28768812del , CM000676.2:g.28768809_28768812del GRCh38
NC_000014.8:g.29238015_29238018del , CM000676.1:g.29238015_29238018del GRCh37
NC_000014.7:g.28307766_28307769del NCBI36
NG_009367.1:g.6729_6732del

Transcript Alleles

HGVS Amino-acid Change
ENST00000706482.1:c.*60_*63del ENSP00000516406.1:n.*60_*63del
ENST00000313071.7:c.*60_*63del MANE Select ENSP00000339004.3:n.*60_*63del
ENST00000313071.6:c.*60_*63del ENSP00000339004.3:n.*60_*63del
NM_005249.4:c.*60_*63del NP_005240.3:n.*60_*63del
NM_005249.5:c.*60_*63del MANE Select NP_005240.3:n.*60_*63del