Canonical Allele Identifier: CA652699090
Gene: IFNW1 HGNC NCBI

Linked Data

COSMIC: COSN20223328
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.21140714_21140715insA , CM000671.2:g.21140714_21140715insA GRCh38
NC_000009.11:g.21140713_21140714insA , CM000671.1:g.21140713_21140714insA GRCh37
NC_000009.10:g.21130713_21130714insA NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000380229.4:c.*268_*269insT MANE Select ENSP00000369578.2:n.*268_*269insT
ENST00000380229.3:c.*268_*269insT ENSP00000369578.2:n.*268_*269insT
NM_002177.1:c.*268_*269insT NP_002168.1:n.*268_*269insT
NM_002177.2:c.*268_*269insT NP_002168.1:n.*268_*269insT
NM_002177.3:c.*268_*269insT MANE Select NP_002168.1:n.*268_*269insT
Search 100 bp 5'
Search 100 bp 3'