Canonical Allele Identifier: CA1583185075

Gene: IRF1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132483932_132483940delinsGAGGGGCCC , CM000667.2:g.132483932_132483940delinsGAGGGGCCC	GRCh38
NC_000005.9:g.131819624_131819632delinsGAGGGGCCC , CM000667.1:g.131819624_131819632delinsGAGGGGCCC	GRCh37
NC_000005.8:g.131847523_131847531delinsGAGGGGCCC	NCBI36
NG_011450.1:g.11834_11842delinsGGGCCCCTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000245414.9:c.*11_*19delinsGGGCCCCTC MANE Select	ENSP00000245414.4:n.*11_*19delinsGGGCCCCTC
ENST00000638452.2:c.-169+34243_-169+34251delinsGAGGGGCCC	ENSP00000492349.2:n.-169+34243_-169+34251delinsGAGGGGCCC
ENST00000638504.1:n.206+63992_206+64000delinsGAGGGGCCC
ENST00000638568.2:c.-311+34243_-311+34251delinsGAGGGGCCC	ENSP00000491158.2:n.-311+34243_-311+34251delinsGAGGGGCCC
ENST00000639899.1:n.289+34243_289+34251delinsGAGGGGCCC
ENST00000640655.2:c.-637-2260_-637-2252delinsGAGGGGCCC	ENSP00000491596.2:n.-637-2260_-637-2252delinsGAGGGGCCC
ENST00000679786.1:n.130+2617_130+2625delinsGGGCCCCTC
ENST00000679921.1:c.292+2617_292+2625delinsGGGCCCCTC	ENSP00000505766.1:n.292+2617_292+2625delinsGGGCCCCTC
ENST00000679945.1:n.130+2617_130+2625delinsGGGCCCCTC
ENST00000679964.1:n.50+1727_50+1735delinsGGGCCCCTC
ENST00000680139.1:c.*11_*19delinsGGGCCCCTC	ENSP00000506148.1:n.*11_*19delinsGGGCCCCTC
ENST00000680380.1:n.136+422_136+430delinsGGGCCCCTC
ENST00000680562.1:c.437_445delinsGGGCCCCTC	ENSP00000505853.1:n.437_445delinsGGGCCCCTC
ENST00000680594.1:n.136+422_136+430delinsGGGCCCCTC
ENST00000680903.1:c.*11_*19delinsGGGCCCCTC	ENSP00000505720.1:n.*11_*19delinsGGGCCCCTC
ENST00000681049.1:n.50+1727_50+1735delinsGGGCCCCTC
ENST00000681240.1:c.239_247delinsGGGCCCCTC	ENSP00000506034.1:n.239_247delinsGGGCCCCTC
ENST00000681336.1:c.236_244delinsGGGCCCCTC	ENSP00000505242.1:n.236_244delinsGGGCCCCTC
ENST00000681634.1:n.136+422_136+430delinsGGGCCCCTC
ENST00000681694.1:c.301_309delinsGGGCCCCTC	ENSP00000506552.1:n.301_309delinsGGGCCCCTC
ENST00000245414.8:c.*11_*19delinsGGGCCCCTC	ENSP00000245414.4:n.*11_*19delinsGGGCCCCTC
ENST00000405885.6:c.*11_*19delinsGGGCCCCTC	ENSP00000384406.1:n.*11_*19delinsGGGCCCCTC
ENST00000472045.1:n.4298_4306delinsGGGCCCCTC
NM_002198.2:c.*11_*19delinsGGGCCCCTC	NP_002189.1:n.*11_*19delinsGGGCCCCTC
XM_011543378.1:c.*11_*19delinsGGGCCCCTC	XP_011541680.1:n.*11_*19delinsGGGCCCCTC
XM_011543379.1:c.*11_*19delinsGGGCCCCTC	XP_011541681.1:n.*11_*19delinsGGGCCCCTC
XR_427711.2:n.1050_1058delinsGGGCCCCTC
NM_001354924.1:c.*11_*19delinsGGGCCCCTC	NP_001341853.1:n.*11_*19delinsGGGCCCCTC
NM_001354925.1:c.*11_*19delinsGGGCCCCTC	NP_001341854.1:n.*11_*19delinsGGGCCCCTC
NR_149068.1:n.1050_1058delinsGGGCCCCTC
XM_011543379.2:c.*11_*19delinsGGGCCCCTC	XP_011541681.1:n.*11_*19delinsGGGCCCCTC
NM_002198.3:c.*11_*19delinsGGGCCCCTC MANE Select	NP_002189.1:n.*11_*19delinsGGGCCCCTC