Canonical Allele Identifier: CA2125999325
Gene: FOXG1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.28767680_28767681delinsCG , CM000676.2:g.28767680_28767681delinsCG GRCh38
NC_000014.8:g.29236886_29236887delinsCG , CM000676.1:g.29236886_29236887delinsCG GRCh37
NC_000014.7:g.28306637_28306638delinsCG NCBI36
NG_009367.1:g.5600_5601delinsCG

Transcript Alleles

HGVS Amino-acid Change
ENST00000706482.1:c.401_402delinsCG ENSP00000516406.1:p.Pro134=
ENST00000313071.7:c.401_402delinsCG MANE Select ENSP00000339004.3:p.Pro134=
ENST00000313071.6:c.401_402delinsCG ENSP00000339004.3:p.Pro134=
NM_005249.4:c.401_402delinsCG NP_005240.3:p.Pro134=
NM_005249.5:c.401_402delinsCG MANE Select NP_005240.3:p.Pro134=
Search 100 bp 5'
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