Canonical Allele Identifier: CA7140700
Gene: FOXG1 HGNC NCBI

Linked Data

dbSNP Id: rs756488909
ExAC: 14:29237980 G / GA
gnomAD v2: 14-29237980-G-GA
gnomAD v4: 14-28768774-G-GA
MyVariant Identifiers: chr14:g.29237980_29237981insA (hg19) chr14:g.28768774_28768775insA (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.28768776dup , CM000676.2:g.28768776dup GRCh38
NC_000014.8:g.29237982dup , CM000676.1:g.29237982dup GRCh37
NC_000014.7:g.28307733dup NCBI36
NG_009367.1:g.6696dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000706482.1:c.*27dup ENSP00000516406.1:n.*27dup
ENST00000313071.7:c.*27dup MANE Select ENSP00000339004.3:n.*27dup
ENST00000313071.6:c.*27dup ENSP00000339004.3:n.*27dup
NM_005249.4:c.*27dup NP_005240.3:n.*27dup
NM_005249.5:c.*27dup MANE Select NP_005240.3:n.*27dup
Search 100 bp 5'
Search 100 bp 3'