Canonical Allele Identifier: CA2321543488
Gene: NFILZ HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.8679472_8679473delinsTG , CM000681.2:g.8679472_8679473delinsTG GRCh38
NC_000019.9:g.8789736_8789737delinsTG , CM000681.1:g.8789736_8789737delinsTG GRCh37
NC_000019.8:g.8650736_8650737delinsTG NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000570582.4:c.*1837_*1838delinsTG ENSP00000500121.1:n.*1837_*1838delinsTG
ENST00000671902.2:c.*1837_*1838delinsTG ENSP00000500604.1:n.*1837_*1838delinsTG
ENST00000673603.2:c.*1837_*1838delinsTG ENSP00000499970.1:n.*1837_*1838delinsTG
ENST00000691075.1:c.*1837_*1838delinsTG MANE Select ENSP00000509575.1:n.*1837_*1838delinsTG
NM_001378599.1:c.*1837_*1838delinsTG NP_001365528.1:n.*1837_*1838delinsTG
NM_001378600.1:c.*1837_*1838delinsTG MANE Select NP_001365529.1:n.*1837_*1838delinsTG
NM_001378601.1:c.*1837_*1838delinsTG NP_001365530.1:n.*1837_*1838delinsTG
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