Canonical Allele Identifier: CA2547798871
Gene: NFILZ HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.8679464A>G , CM000681.2:g.8679464A>G GRCh38
NC_000019.9:g.8789728A>G , CM000681.1:g.8789728A>G GRCh37
NC_000019.8:g.8650728A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000570582.4:c.*1829A>G ENSP00000500121.1:n.*1829A>G
ENST00000671902.2:c.*1829A>G ENSP00000500604.1:n.*1829A>G
ENST00000673603.2:c.*1829A>G ENSP00000499970.1:n.*1829A>G
ENST00000691075.1:c.*1829A>G MANE Select ENSP00000509575.1:n.*1829A>G
NM_001378599.1:c.*1829A>G NP_001365528.1:n.*1829A>G
NM_001378600.1:c.*1829A>G MANE Select NP_001365529.1:n.*1829A>G
NM_001378601.1:c.*1829A>G NP_001365530.1:n.*1829A>G
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