Canonical Allele Identifier: CA389475144
Gene: FOXG1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.28767742G>A , CM000676.2:g.28767742G>A GRCh38
NC_000014.8:g.29236948G>A , CM000676.1:g.29236948G>A GRCh37
NC_000014.7:g.28306699G>A NCBI36
NG_009367.1:g.5662G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000706482.1:c.463G>A ENSP00000516406.1:p.Glu155Lys
ENST00000313071.7:c.463G>A MANE Select ENSP00000339004.3:p.Glu155Lys
ENST00000313071.6:c.463G>A ENSP00000339004.3:p.Glu155Lys
NM_005249.4:c.463G>A NP_005240.3:p.Glu155Lys
NM_005249.5:c.463G>A MANE Select NP_005240.3:p.Glu155Lys