Canonical Allele Identifier: CA389476483
Gene: FOXG1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.28768352C>A , CM000676.2:g.28768352C>A GRCh38
NC_000014.8:g.29237558C>A , CM000676.1:g.29237558C>A GRCh37
NC_000014.7:g.28307309C>A NCBI36
NG_009367.1:g.6272C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000706482.1:c.1073C>A ENSP00000516406.1:p.Thr358Asn
ENST00000313071.7:c.1073C>A MANE Select ENSP00000339004.3:p.Thr358Asn
ENST00000313071.6:c.1073C>A ENSP00000339004.3:p.Thr358Asn
NM_005249.4:c.1073C>A NP_005240.3:p.Thr358Asn
NM_005249.5:c.1073C>A MANE Select NP_005240.3:p.Thr358Asn