Canonical Allele Identifier: CA486098060
Gene: FOXG1 HGNC NCBI

Linked Data

dbSNP Id: rs1555321234
MyVariant Identifiers: chr14:g.29236692del (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.28767486del , CM000676.2:g.28767486del GRCh38
NC_000014.8:g.29236692del , CM000676.1:g.29236692del GRCh37
NC_000014.7:g.28306443del NCBI36
NG_009367.1:g.5406del

Transcript Alleles

HGVS Amino-acid Change
ENST00000706482.1:c.207del ENSP00000516406.1:p.Gln70SerfsTer?
ENST00000313071.7:c.207del MANE Select ENSP00000339004.3:p.Gln70SerfsTer?
ENST00000313071.6:c.207del ENSP00000339004.3:p.Gln70SerfsTer?
NM_005249.4:c.207del NP_005240.3:p.Gln70SerfsTer?
NM_005249.5:c.207del MANE Select NP_005240.3:p.Gln70SerfsTer?