Canonical Allele Identifier: CA961430588
Gene: FOXG1 HGNC NCBI

Linked Data

dbSNP Id: rs1881830428

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.28768788_28768789del , CM000676.2:g.28768788_28768789del GRCh38
NC_000014.8:g.29237994_29237995del , CM000676.1:g.29237994_29237995del GRCh37
NC_000014.7:g.28307745_28307746del NCBI36
NG_009367.1:g.6708_6709del

Transcript Alleles

HGVS Amino-acid Change
ENST00000706482.1:c.*39_*40del ENSP00000516406.1:n.*39_*40del
ENST00000313071.7:c.*39_*40del MANE Select ENSP00000339004.3:n.*39_*40del
ENST00000313071.6:c.*39_*40del ENSP00000339004.3:n.*39_*40del
NM_005249.4:c.*39_*40del NP_005240.3:n.*39_*40del
NM_005249.5:c.*39_*40del MANE Select NP_005240.3:n.*39_*40del