Canonical Allele Identifier: CA2126000416
Gene: FOXG1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.28768438_28768440delinsTCG , CM000676.2:g.28768438_28768440delinsTCG GRCh38
NC_000014.8:g.29237644_29237646delinsTCG , CM000676.1:g.29237644_29237646delinsTCG GRCh37
NC_000014.7:g.28307395_28307397delinsTCG NCBI36
NG_009367.1:g.6358_6360delinsTCG

Transcript Alleles

HGVS Amino-acid change
ENST00000706482.1:c.1159_1161delinsTCG ENSP00000516406.1:p.Ser387=
ENST00000313071.7:c.1159_1161delinsTCG MANE Select ENSP00000339004.3:p.Ser387=
ENST00000313071.6:c.1159_1161delinsTCG ENSP00000339004.3:p.Ser387=
NM_005249.4:c.1159_1161delinsTCG NP_005240.3:p.Ser387=
NM_005249.5:c.1159_1161delinsTCG MANE Select NP_005240.3:p.Ser387=