Canonical Allele Identifier: CA258396609
Gene: FOXG1 HGNC NCBI

Linked Data

dbSNP Id: rs962190178
gnomAD v3: 14-28768810-TA-T
gnomAD v4: 14-28768810-TA-T
COSMIC: COSN18737993 COSN18737994
MyVariant Identifiers: chr14:g.29238017del (hg19) chr14:g.28768811del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.28768817del , CM000676.2:g.28768817del GRCh38
NC_000014.8:g.29238023del , CM000676.1:g.29238023del GRCh37
NC_000014.7:g.28307774del NCBI36
NG_009367.1:g.6737del

Transcript Alleles

HGVS Amino-acid Change
ENST00000706482.1:c.*68del ENSP00000516406.1:n.*68del
ENST00000313071.7:c.*68del MANE Select ENSP00000339004.3:n.*68del
ENST00000313071.6:c.*68del ENSP00000339004.3:n.*68del
NM_005249.4:c.*68del NP_005240.3:n.*68del
NM_005249.5:c.*68del MANE Select NP_005240.3:n.*68del
Search 100 bp 5'
Search 100 bp 3'