Canonical Allele Identifier: CA16043741
Gene: FOXG1 HGNC NCBI

Linked Data

ClinVar Variation Id: 374450
ClinVar RCV Id: RCV000416103
dbSNP Id: rs1555321369
MyVariant Identifiers: chr14:g.29237370dup (hg19) chr14:g.28768164dup (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.28768164dup , CM000676.2:g.28768164dup GRCh38
NC_000014.8:g.29237370dup , CM000676.1:g.29237370dup GRCh37
NC_000014.7:g.28307121dup NCBI36
NG_009367.1:g.6084dup

Transcript Alleles

HGVS Amino-acid change
ENST00000706482.1:c.885dup ENSP00000516406.1:p.Gly296ArgfsTer?
ENST00000313071.7:c.885dup MANE Select ENSP00000339004.3:p.Gly296ArgfsTer?
ENST00000313071.6:c.885dup ENSP00000339004.3:p.Gly296ArgfsTer?
NM_005249.4:c.885dup NP_005240.3:p.Gly296ArgfsTer?
NM_005249.5:c.885dup MANE Select NP_005240.3:p.Gly296ArgfsTer?
Search 100 bp 5'
Search 100 bp 3'