Canonical Allele Identifier: CA1081639269
Gene: IRF1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.132483610del , CM000667.2:g.132483610del GRCh38
NC_000005.9:g.131819302del , CM000667.1:g.131819302del GRCh37
NC_000005.8:g.131847201del NCBI36
NG_011450.1:g.12167del

Transcript Alleles

HGVS Amino-acid Change
ENST00000245414.9:c.*344del MANE Select ENSP00000245414.4:n.*344del
ENST00000638452.2:c.-169+33921del ENSP00000492349.2:n.-169+33921del
ENST00000638504.1:n.206+63670del
ENST00000638568.2:c.-311+33921del ENSP00000491158.2:n.-311+33921del
ENST00000639899.1:n.289+33921del
ENST00000640655.2:c.-637-2582del ENSP00000491596.2:n.-637-2582del
ENST00000679786.1:n.130+2950del
ENST00000679921.1:c.292+2950del ENSP00000505766.1:n.292+2950del
ENST00000679945.1:n.130+2950del
ENST00000679964.1:n.50+2060del
ENST00000680380.1:n.136+755del
ENST00000680594.1:n.136+755del
ENST00000681049.1:n.50+2060del
ENST00000681634.1:n.136+755del
ENST00000245414.8:c.*344del ENSP00000245414.4:n.*344del
ENST00000405885.6:c.*344del ENSP00000384406.1:n.*344del
ENST00000472045.1:n.4631del
NM_002198.2:c.*344del NP_002189.1:n.*344del
XM_011543378.1:c.*344del XP_011541680.1:n.*344del
XM_011543379.1:c.*344del XP_011541681.1:n.*344del
XR_427711.2:n.1383del
NM_001354924.1:c.*344del NP_001341853.1:n.*344del
NM_001354925.1:c.*344del NP_001341854.1:n.*344del
NR_149068.1:n.1383del
XM_011543379.2:c.*344del XP_011541681.1:n.*344del
NM_002198.3:c.*344del MANE Select NP_002189.1:n.*344del