Canonical Allele Identifier: CA2126000550
Gene: FOXG1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.28768792T= , CM000676.2:g.28768792T= GRCh38
NC_000014.8:g.29237998T= , CM000676.1:g.29237998T= GRCh37
NC_000014.7:g.28307749T= NCBI36
NG_009367.1:g.6712T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000706482.1:c.*43T= ENSP00000516406.1:n.*43T=
ENST00000313071.7:c.*43T= MANE Select ENSP00000339004.3:n.*43T=
ENST00000313071.6:c.*43T= ENSP00000339004.3:n.*43T=
NM_005249.4:c.*43T= NP_005240.3:n.*43T=
NM_005249.5:c.*43T= MANE Select NP_005240.3:n.*43T=
Search 100 bp 5'
Search 100 bp 3'