Canonical Allele Identifier: CA2126000576
Gene: FOXG1 HGNC NCBI

Linked Data

dbSNP Id: rs1881831930

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.28768850_28768851del , CM000676.2:g.28768850_28768851del GRCh38
NC_000014.8:g.29238056_29238057del , CM000676.1:g.29238056_29238057del GRCh37
NC_000014.7:g.28307807_28307808del NCBI36
NG_009367.1:g.6770_6771del

Transcript Alleles

HGVS Amino-acid Change
ENST00000706482.1:c.*101_*102del ENSP00000516406.1:n.*101_*102del
ENST00000313071.7:c.*101_*102del MANE Select ENSP00000339004.3:n.*101_*102del
ENST00000313071.6:c.*101_*102del ENSP00000339004.3:n.*101_*102del
NM_005249.4:c.*101_*102del NP_005240.3:n.*101_*102del
NM_005249.5:c.*101_*102del MANE Select NP_005240.3:n.*101_*102del