Canonical Allele Identifier: CA655705553
Gene: FOXG1 HGNC NCBI

Linked Data

gnomAD v4: 14-28768810-TAAAA-T
COSMIC: COSN508321 COSN508322
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.28768814_28768817del , CM000676.2:g.28768814_28768817del GRCh38
NC_000014.8:g.29238020_29238023del , CM000676.1:g.29238020_29238023del GRCh37
NC_000014.7:g.28307771_28307774del NCBI36
NG_009367.1:g.6734_6737del

Transcript Alleles

HGVS Amino-acid Change
ENST00000706482.1:c.*65_*68del ENSP00000516406.1:n.*65_*68del
ENST00000313071.7:c.*65_*68del MANE Select ENSP00000339004.3:n.*65_*68del
ENST00000313071.6:c.*65_*68del ENSP00000339004.3:n.*65_*68del
NM_005249.4:c.*65_*68del NP_005240.3:n.*65_*68del
NM_005249.5:c.*65_*68del MANE Select NP_005240.3:n.*65_*68del
Search 100 bp 5'
Search 100 bp 3'