Canonical Allele Identifier: CA920052895
Gene: NFILZ HGNC NCBI

Linked Data

dbSNP Id: rs797044346
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.8679457_8679458delinsTG , CM000681.2:g.8679457_8679458delinsTG GRCh38
NC_000019.9:g.8789721_8789722delinsTG , CM000681.1:g.8789721_8789722delinsTG GRCh37
NC_000019.8:g.8650721_8650722delinsTG NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000570582.4:c.*1822_*1823delinsTG ENSP00000500121.1:n.*1822_*1823delinsTG
ENST00000671902.2:c.*1822_*1823delinsTG ENSP00000500604.1:n.*1822_*1823delinsTG
ENST00000673603.2:c.*1822_*1823delinsTG ENSP00000499970.1:n.*1822_*1823delinsTG
ENST00000691075.1:c.*1822_*1823delinsTG MANE Select ENSP00000509575.1:n.*1822_*1823delinsTG
NM_001378599.1:c.*1822_*1823delinsTG NP_001365528.1:n.*1822_*1823delinsTG
NM_001378600.1:c.*1822_*1823delinsTG MANE Select NP_001365529.1:n.*1822_*1823delinsTG
NM_001378601.1:c.*1822_*1823delinsTG NP_001365530.1:n.*1822_*1823delinsTG
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