Canonical Allele Identifier: CA1838717716
Gene: IFNW1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.21140713_21140714delinsTG , CM000671.2:g.21140713_21140714delinsTG GRCh38
NC_000009.11:g.21140712_21140713delinsTG , CM000671.1:g.21140712_21140713delinsTG GRCh37
NC_000009.10:g.21130712_21130713delinsTG NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000380229.4:c.*269_*270delinsCA MANE Select ENSP00000369578.2:n.*269_*270delinsCA
ENST00000380229.3:c.*269_*270delinsCA ENSP00000369578.2:n.*269_*270delinsCA
NM_002177.1:c.*269_*270delinsCA NP_002168.1:n.*269_*270delinsCA
NM_002177.2:c.*269_*270delinsCA NP_002168.1:n.*269_*270delinsCA
NM_002177.3:c.*269_*270delinsCA MANE Select NP_002168.1:n.*269_*270delinsCA
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