Canonical Allele Identifier: CA2575498220
Gene: FOXG1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.28768834_28768835del , CM000676.2:g.28768834_28768835del GRCh38
NC_000014.8:g.29238040_29238041del , CM000676.1:g.29238040_29238041del GRCh37
NC_000014.7:g.28307791_28307792del NCBI36
NG_009367.1:g.6754_6755del

Transcript Alleles

HGVS Amino-acid Change
ENST00000706482.1:c.*85_*86del ENSP00000516406.1:n.*85_*86del
ENST00000313071.7:c.*85_*86del MANE Select ENSP00000339004.3:n.*85_*86del
ENST00000313071.6:c.*85_*86del ENSP00000339004.3:n.*85_*86del
NM_005249.4:c.*85_*86del NP_005240.3:n.*85_*86del
NM_005249.5:c.*85_*86del MANE Select NP_005240.3:n.*85_*86del