Canonical Allele Identifier: CA1583185097

Gene: IRF1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132483988C= , CM000667.2:g.132483988C=	GRCh38
NC_000005.9:g.131819680C= , CM000667.1:g.131819680C=	GRCh37
NC_000005.8:g.131847579C=	NCBI36
NG_011450.1:g.11786G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000245414.9:c.941G= MANE Select	ENSP00000245414.4:p.Arg314=
ENST00000638452.2:c.-169+34299C=	ENSP00000492349.2:n.-169+34299C=
ENST00000638504.1:n.206+64048C=
ENST00000638568.2:c.-311+34299C=	ENSP00000491158.2:n.-311+34299C=
ENST00000639899.1:n.289+34299C=
ENST00000640655.2:c.-637-2204C=	ENSP00000491596.2:n.-637-2204C=
ENST00000679743.1:c.562G=	ENSP00000505257.1:n.562G=
ENST00000679786.1:n.130+2569G=
ENST00000679860.1:c.229G=
ENST00000679921.1:c.292+2569G=	ENSP00000505766.1:n.292+2569G=
ENST00000679945.1:n.130+2569G=
ENST00000679964.1:n.50+1679G=
ENST00000680139.1:c.755G=	ENSP00000506148.1:p.Arg252=
ENST00000680380.1:n.136+374G=
ENST00000680562.1:c.389G=	ENSP00000505853.1:p.Arg130=
ENST00000680594.1:n.136+374G=
ENST00000680903.1:c.818G=	ENSP00000505720.1:p.Arg273=
ENST00000681049.1:n.50+1679G=
ENST00000681240.1:c.191G=	ENSP00000506034.1:p.Arg64=
ENST00000681336.1:c.188G=	ENSP00000505242.1:p.Arg63=
ENST00000681462.1:c.778G=
ENST00000681595.1:c.502G=	ENSP00000506023.1:n.502G=
ENST00000681634.1:n.136+374G=
ENST00000681694.1:c.253G=	ENSP00000506552.1:n.253G=
ENST00000681715.1:c.439G=	ENSP00000506545.1:n.439G=
ENST00000245414.8:c.941G=	ENSP00000245414.4:p.Arg314=
ENST00000405885.6:c.941G=	ENSP00000384406.1:p.Arg314=
ENST00000472045.1:n.4250G=
NM_002198.2:c.941G=	NP_002189.1:p.Arg314=
XM_011543378.1:c.818G=	XP_011541680.1:p.Arg273=
XM_011543379.1:c.689G=	XP_011541681.1:p.Arg230=
XR_427711.2:n.1002G=
NM_001354924.1:c.818G=	NP_001341853.1:p.Arg273=
NM_001354925.1:c.755G=	NP_001341854.1:p.Arg252=
NR_149068.1:n.1002G=
XM_011543379.2:c.689G=	XP_011541681.1:p.Arg230=
NM_002198.3:c.941G= MANE Select	NP_002189.1:p.Arg314=