Canonical Allele Identifier: CA2575498161
Gene: FOXG1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.28767491_28767502dup , CM000676.2:g.28767491_28767502dup GRCh38
NC_000014.8:g.29236697_29236708dup , CM000676.1:g.29236697_29236708dup GRCh37
NC_000014.7:g.28306448_28306459dup NCBI36
NG_009367.1:g.5411_5422dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000706482.1:c.212_223dup ENSP00000516406.1:p.Pro74_Pro75insGlnGlnGlnPro
ENST00000313071.7:c.212_223dup MANE Select ENSP00000339004.3:p.Pro74_Pro75insGlnGlnGlnPro
ENST00000313071.6:c.212_223dup ENSP00000339004.3:p.Pro74_Pro75insGlnGlnGlnPro
NM_005249.4:c.212_223dup NP_005240.3:p.Pro74_Pro75insGlnGlnGlnPro
NM_005249.5:c.212_223dup MANE Select NP_005240.3:p.Pro74_Pro75insGlnGlnGlnPro
Search 100 bp 5'
Search 100 bp 3'