Canonical Allele Identifier: CA2801003669
Gene: FOXG1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.28767612_28767613del , CM000676.2:g.28767612_28767613del GRCh38
NC_000014.8:g.29236818_29236819del , CM000676.1:g.29236818_29236819del GRCh37
NC_000014.7:g.28306569_28306570del NCBI36
NG_009367.1:g.5532_5533del

Transcript Alleles

HGVS Amino-acid Change
ENST00000706482.1:c.333_334del ENSP00000516406.1:p.Pro112GlyfsTer8
ENST00000313071.7:c.333_334del MANE Select ENSP00000339004.3:p.Pro112GlyfsTer8
ENST00000313071.6:c.333_334del ENSP00000339004.3:p.Pro112GlyfsTer8
NM_005249.4:c.333_334del NP_005240.3:p.Pro112GlyfsTer8
NM_005249.5:c.333_334del MANE Select NP_005240.3:p.Pro112GlyfsTer8
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