Canonical Allele Identifier: CA1583185089

Gene: IRF1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132483955G= , CM000667.2:g.132483955G=	GRCh38
NC_000005.9:g.131819647G= , CM000667.1:g.131819647G=	GRCh37
NC_000005.8:g.131847546G=	NCBI36
NG_011450.1:g.11819C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000245414.9:c.974C= MANE Select	ENSP00000245414.4:p.Pro325=
ENST00000638452.2:c.-169+34266G=	ENSP00000492349.2:n.-169+34266G=
ENST00000638504.1:n.206+64015G=
ENST00000638568.2:c.-311+34266G=	ENSP00000491158.2:n.-311+34266G=
ENST00000639899.1:n.289+34266G=
ENST00000640655.2:c.-637-2237G=	ENSP00000491596.2:n.-637-2237G=
ENST00000679743.1:c.595C=	ENSP00000505257.1:n.595C=
ENST00000679786.1:n.130+2602C=
ENST00000679921.1:c.292+2602C=	ENSP00000505766.1:n.292+2602C=
ENST00000679945.1:n.130+2602C=
ENST00000679964.1:n.50+1712C=
ENST00000680139.1:c.788C=	ENSP00000506148.1:p.Pro263=
ENST00000680380.1:n.136+407C=
ENST00000680562.1:c.422C=	ENSP00000505853.1:p.Pro141=
ENST00000680594.1:n.136+407C=
ENST00000680903.1:c.851C=	ENSP00000505720.1:p.Pro284=
ENST00000681049.1:n.50+1712C=
ENST00000681240.1:c.224C=	ENSP00000506034.1:p.Pro75=
ENST00000681336.1:c.221C=	ENSP00000505242.1:p.Pro74=
ENST00000681595.1:c.535C=	ENSP00000506023.1:n.535C=
ENST00000681634.1:n.136+407C=
ENST00000681694.1:c.286C=	ENSP00000506552.1:n.286C=
ENST00000681715.1:c.472C=	ENSP00000506545.1:n.472C=
ENST00000245414.8:c.974C=	ENSP00000245414.4:p.Pro325=
ENST00000405885.6:c.974C=	ENSP00000384406.1:p.Pro325=
ENST00000472045.1:n.4283C=
NM_002198.2:c.974C=	NP_002189.1:p.Pro325=
XM_011543378.1:c.851C=	XP_011541680.1:p.Pro284=
XM_011543379.1:c.722C=	XP_011541681.1:p.Pro241=
XR_427711.2:n.1035C=
NM_001354924.1:c.851C=	NP_001341853.1:p.Pro284=
NM_001354925.1:c.788C=	NP_001341854.1:p.Pro263=
NR_149068.1:n.1035C=
XM_011543379.2:c.722C=	XP_011541681.1:p.Pro241=
NM_002198.3:c.974C= MANE Select	NP_002189.1:p.Pro325=