Canonical Allele Identifier: CA961450454
Gene: FOXG1 HGNC NCBI

Linked Data

gnomAD v3: 14-28767591-C-CCAG
gnomAD v4: 14-28767591-C-CCAG
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.28767592_28767593insAGC , CM000676.2:g.28767592_28767593insAGC GRCh38
NC_000014.8:g.29236798_29236799insAGC , CM000676.1:g.29236798_29236799insAGC GRCh37
NC_000014.7:g.28306549_28306550insAGC NCBI36
NG_009367.1:g.5512_5513insAGC

Transcript Alleles

HGVS Amino-acid change
ENST00000706482.1:c.313_314insAGC ENSP00000516406.1:p.Leu104_Pro105insGln
ENST00000313071.7:c.313_314insAGC MANE Select ENSP00000339004.3:p.Leu104_Pro105insGln
ENST00000313071.6:c.313_314insAGC ENSP00000339004.3:p.Leu104_Pro105insGln
NM_005249.4:c.313_314insAGC NP_005240.3:p.Leu104_Pro105insGln
NM_005249.5:c.313_314insAGC MANE Select NP_005240.3:p.Leu104_Pro105insGln
Search 100 bp 5'
Search 100 bp 3'