Canonical Allele Identifier: CA2126000554
Gene: FOXG1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.28768810_28768811delinsTA , CM000676.2:g.28768810_28768811delinsTA GRCh38
NC_000014.8:g.29238016_29238017delinsTA , CM000676.1:g.29238016_29238017delinsTA GRCh37
NC_000014.7:g.28307767_28307768delinsTA NCBI36
NG_009367.1:g.6730_6731delinsTA

Transcript Alleles

HGVS Amino-acid Change
ENST00000706482.1:c.*61_*62delinsTA ENSP00000516406.1:n.*61_*62delinsTA
ENST00000313071.7:c.*61_*62delinsTA MANE Select ENSP00000339004.3:n.*61_*62delinsTA
ENST00000313071.6:c.*61_*62delinsTA ENSP00000339004.3:n.*61_*62delinsTA
NM_005249.4:c.*61_*62delinsTA NP_005240.3:n.*61_*62delinsTA
NM_005249.5:c.*61_*62delinsTA MANE Select NP_005240.3:n.*61_*62delinsTA
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