Canonical Allele Identifier: CA2125998881
Gene: FOXG1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.28767503_28767505delinsCGC , CM000676.2:g.28767503_28767505delinsCGC GRCh38
NC_000014.8:g.29236709_29236711delinsCGC , CM000676.1:g.29236709_29236711delinsCGC GRCh37
NC_000014.7:g.28306460_28306462delinsCGC NCBI36
NG_009367.1:g.5423_5425delinsCGC

Transcript Alleles

HGVS Amino-acid Change
ENST00000706482.1:c.224_226delinsCGC ENSP00000516406.1:p.Pro75=
ENST00000313071.7:c.224_226delinsCGC MANE Select ENSP00000339004.3:p.Pro75=
ENST00000313071.6:c.224_226delinsCGC ENSP00000339004.3:p.Pro75=
NM_005249.4:c.224_226delinsCGC NP_005240.3:p.Pro75=
NM_005249.5:c.224_226delinsCGC MANE Select NP_005240.3:p.Pro75=
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