Canonical Allele Identifier: CA1583184954

Gene: IRF1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132483583_132483584delinsCT , CM000667.2:g.132483583_132483584delinsCT	GRCh38
NC_000005.9:g.131819275_131819276delinsCT , CM000667.1:g.131819275_131819276delinsCT	GRCh37
NC_000005.8:g.131847174_131847175delinsCT	NCBI36
NG_011450.1:g.12190_12191delinsAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000245414.9:c.*367_*368delinsAG MANE Select	ENSP00000245414.4:n.*367_*368delinsAG
ENST00000638452.2:c.-169+33894_-169+33895delinsCT	ENSP00000492349.2:n.-169+33894_-169+33895delinsCT
ENST00000638504.1:n.206+63643_206+63644delinsCT
ENST00000638568.2:c.-311+33894_-311+33895delinsCT	ENSP00000491158.2:n.-311+33894_-311+33895delinsCT
ENST00000639899.1:n.289+33894_289+33895delinsCT
ENST00000640655.2:c.-637-2609_-637-2608delinsCT	ENSP00000491596.2:n.-637-2609_-637-2608delinsCT
ENST00000679786.1:n.130+2973_130+2974delinsAG
ENST00000679921.1:c.292+2973_292+2974delinsAG	ENSP00000505766.1:n.292+2973_292+2974delinsAG
ENST00000679945.1:n.130+2973_130+2974delinsAG
ENST00000679964.1:n.50+2083_50+2084delinsAG
ENST00000680380.1:n.136+778_136+779delinsAG
ENST00000680594.1:n.136+778_136+779delinsAG
ENST00000681049.1:n.50+2083_50+2084delinsAG
ENST00000681634.1:n.136+778_136+779delinsAG
ENST00000245414.8:c.*367_*368delinsAG	ENSP00000245414.4:n.*367_*368delinsAG
ENST00000405885.6:c.*367_*368delinsAG	ENSP00000384406.1:n.*367_*368delinsAG
ENST00000472045.1:n.4654_4655delinsAG
NM_002198.2:c.*367_*368delinsAG	NP_002189.1:n.*367_*368delinsAG
XM_011543378.1:c.*367_*368delinsAG	XP_011541680.1:n.*367_*368delinsAG
XM_011543379.1:c.*367_*368delinsAG	XP_011541681.1:n.*367_*368delinsAG
XR_427711.2:n.1406_1407delinsAG
NM_001354924.1:c.*367_*368delinsAG	NP_001341853.1:n.*367_*368delinsAG
NM_001354925.1:c.*367_*368delinsAG	NP_001341854.1:n.*367_*368delinsAG
NR_149068.1:n.1406_1407delinsAG
XM_011543379.2:c.*367_*368delinsAG	XP_011541681.1:n.*367_*368delinsAG
NM_002198.3:c.*367_*368delinsAG MANE Select	NP_002189.1:n.*367_*368delinsAG