Canonical Allele Identifier: CA2125998856
Gene: FOXG1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.28767476_28767497delinsCGCCGCCGCCGCAGCAGCAGCA , CM000676.2:g.28767476_28767497delinsCGCCGCCGCCGCAGCAGCAGCA GRCh38
NC_000014.8:g.29236682_29236703delinsCGCCGCCGCCGCAGCAGCAGCA , CM000676.1:g.29236682_29236703delinsCGCCGCCGCCGCAGCAGCAGCA GRCh37
NC_000014.7:g.28306433_28306454delinsCGCCGCCGCCGCAGCAGCAGCA NCBI36
NG_009367.1:g.5396_5417delinsCGCCGCCGCCGCAGCAGCAGCA

Transcript Alleles

HGVS Amino-acid Change
ENST00000706482.1:c.197_218delinsCGCCGCCGCCGCAGCAGCAGCA ENSP00000516406.1:p.Pro66=
ENST00000313071.7:c.197_218delinsCGCCGCCGCCGCAGCAGCAGCA MANE Select ENSP00000339004.3:p.Pro66=
ENST00000313071.6:c.197_218delinsCGCCGCCGCCGCAGCAGCAGCA ENSP00000339004.3:p.Pro66=
NM_005249.4:c.197_218delinsCGCCGCCGCCGCAGCAGCAGCA NP_005240.3:p.Pro66=
NM_005249.5:c.197_218delinsCGCCGCCGCCGCAGCAGCAGCA MANE Select NP_005240.3:p.Pro66=
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