Canonical Allele Identifier: CA2321543478
Gene: NFILZ HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.8679456_8679458delinsCCA , CM000681.2:g.8679456_8679458delinsCCA GRCh38
NC_000019.9:g.8789720_8789722delinsCCA , CM000681.1:g.8789720_8789722delinsCCA GRCh37
NC_000019.8:g.8650720_8650722delinsCCA NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000570582.4:c.*1821_*1823delinsCCA ENSP00000500121.1:n.*1821_*1823delinsCCA
ENST00000671902.2:c.*1821_*1823delinsCCA ENSP00000500604.1:n.*1821_*1823delinsCCA
ENST00000673603.2:c.*1821_*1823delinsCCA ENSP00000499970.1:n.*1821_*1823delinsCCA
ENST00000691075.1:c.*1821_*1823delinsCCA MANE Select ENSP00000509575.1:n.*1821_*1823delinsCCA
NM_001378599.1:c.*1821_*1823delinsCCA NP_001365528.1:n.*1821_*1823delinsCCA
NM_001378600.1:c.*1821_*1823delinsCCA MANE Select NP_001365529.1:n.*1821_*1823delinsCCA
NM_001378601.1:c.*1821_*1823delinsCCA NP_001365530.1:n.*1821_*1823delinsCCA