Canonical Allele Identifier: CA2801003476
Gene: FOXG1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.28768848_28768853del , CM000676.2:g.28768848_28768853del GRCh38
NC_000014.8:g.29238054_29238059del , CM000676.1:g.29238054_29238059del GRCh37
NC_000014.7:g.28307805_28307810del NCBI36
NG_009367.1:g.6768_6773del

Transcript Alleles

HGVS Amino-acid Change
ENST00000706482.1:c.*99_*104del ENSP00000516406.1:n.*99_*104del
ENST00000313071.7:c.*99_*104del MANE Select ENSP00000339004.3:n.*99_*104del
ENST00000313071.6:c.*99_*104del ENSP00000339004.3:n.*99_*104del
NM_005249.4:c.*99_*104del NP_005240.3:n.*99_*104del
NM_005249.5:c.*99_*104del MANE Select NP_005240.3:n.*99_*104del