Canonical Allele Identifier: CA2126000523
Gene: FOXG1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.28768722_28768725delinsGTCT , CM000676.2:g.28768722_28768725delinsGTCT GRCh38
NC_000014.8:g.29237928_29237931delinsGTCT , CM000676.1:g.29237928_29237931delinsGTCT GRCh37
NC_000014.7:g.28307679_28307682delinsGTCT NCBI36
NG_009367.1:g.6642_6645delinsGTCT

Transcript Alleles

HGVS Amino-acid Change
ENST00000706482.1:c.1443_1446delinsGTCT ENSP00000516406.1:p.Gly481=
ENST00000313071.7:c.1443_1446delinsGTCT MANE Select ENSP00000339004.3:p.Gly481=
ENST00000313071.6:c.1443_1446delinsGTCT ENSP00000339004.3:p.Gly481=
NM_005249.4:c.1443_1446delinsGTCT NP_005240.3:p.Gly481=
NM_005249.5:c.1443_1446delinsGTCT MANE Select NP_005240.3:p.Gly481=
Search 100 bp 5'
Search 100 bp 3'