Canonical Allele Identifier: CA2739277845
Gene: FOXG1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2818773
ClinVar RCV Id: RCV003630403
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.28768081_28768083del , CM000676.2:g.28768081_28768083del GRCh38
NC_000014.8:g.29237287_29237289del , CM000676.1:g.29237287_29237289del GRCh37
NC_000014.7:g.28307038_28307040del NCBI36
NG_009367.1:g.6001_6003del

Transcript Alleles

HGVS Amino-acid Change
ENST00000706482.1:c.802_804del ENSP00000516406.1:p.Gly268del
ENST00000313071.7:c.802_804del MANE Select ENSP00000339004.3:p.Gly268del
ENST00000313071.6:c.802_804del ENSP00000339004.3:p.Gly268del
NM_005249.4:c.802_804del NP_005240.3:p.Gly268del
NM_005249.5:c.802_804del MANE Select NP_005240.3:p.Gly268del
Search 100 bp 5'
Search 100 bp 3'