Canonical Allele Identifier: CA2624400772
Gene: FOXG1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.28768846_28768847insT , CM000676.2:g.28768846_28768847insT GRCh38
NC_000014.8:g.29238052_29238053insT , CM000676.1:g.29238052_29238053insT GRCh37
NC_000014.7:g.28307803_28307804insT NCBI36
NG_009367.1:g.6766_6767insT

Transcript Alleles

HGVS Amino-acid Change
ENST00000706482.1:c.*97_*98insT ENSP00000516406.1:n.*97_*98insT
ENST00000313071.7:c.*97_*98insT MANE Select ENSP00000339004.3:n.*97_*98insT
ENST00000313071.6:c.*97_*98insT ENSP00000339004.3:n.*97_*98insT
NM_005249.4:c.*97_*98insT NP_005240.3:n.*97_*98insT
NM_005249.5:c.*97_*98insT MANE Select NP_005240.3:n.*97_*98insT