Canonical Allele Identifier: CA2624400221
Gene: FOXG1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.28768348_28768350del , CM000676.2:g.28768348_28768350del GRCh38
NC_000014.8:g.29237554_29237556del , CM000676.1:g.29237554_29237556del GRCh37
NC_000014.7:g.28307305_28307307del NCBI36
NG_009367.1:g.6268_6270del

Transcript Alleles

HGVS Amino-acid change
ENST00000706482.1:c.1069_1071del ENSP00000516406.1:p.Ser357del
ENST00000313071.7:c.1069_1071del MANE Select ENSP00000339004.3:p.Ser357del
ENST00000313071.6:c.1069_1071del ENSP00000339004.3:p.Ser357del
NM_005249.4:c.1069_1071del NP_005240.3:p.Ser357del
NM_005249.5:c.1069_1071del MANE Select NP_005240.3:p.Ser357del