Canonical Allele Identifier: CA2624398523
Gene: FOXG1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.28767501_28767530del , CM000676.2:g.28767501_28767530del GRCh38
NC_000014.8:g.29236707_29236736del , CM000676.1:g.29236707_29236736del GRCh37
NC_000014.7:g.28306458_28306487del NCBI36
NG_009367.1:g.5421_5450del

Transcript Alleles

HGVS Amino-acid Change
ENST00000706482.1:c.222_251del ENSP00000516406.1:p.Pro75_Pro84del
ENST00000313071.7:c.222_251del MANE Select ENSP00000339004.3:p.Pro75_Pro84del
ENST00000313071.6:c.222_251del ENSP00000339004.3:p.Pro75_Pro84del
NM_005249.4:c.222_251del NP_005240.3:p.Pro75_Pro84del
NM_005249.5:c.222_251del MANE Select NP_005240.3:p.Pro75_Pro84del