Canonical Allele Identifier: CA1583185034

Gene: IRF1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132483806C= , CM000667.2:g.132483806C=	GRCh38
NC_000005.9:g.131819498C= , CM000667.1:g.131819498C=	GRCh37
NC_000005.8:g.131847397C=	NCBI36
NG_011450.1:g.11968G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000245414.9:c.*145G= MANE Select	ENSP00000245414.4:n.*145G=
ENST00000638452.2:c.-169+34117C=	ENSP00000492349.2:n.-169+34117C=
ENST00000638504.1:n.206+63866C=
ENST00000638568.2:c.-311+34117C=	ENSP00000491158.2:n.-311+34117C=
ENST00000639899.1:n.289+34117C=
ENST00000640655.2:c.-637-2386C=	ENSP00000491596.2:n.-637-2386C=
ENST00000679786.1:n.130+2751G=
ENST00000679921.1:c.292+2751G=	ENSP00000505766.1:n.292+2751G=
ENST00000679945.1:n.130+2751G=
ENST00000679964.1:n.50+1861G=
ENST00000680139.1:c.*145G=	ENSP00000506148.1:n.*145G=
ENST00000680380.1:n.136+556G=
ENST00000680594.1:n.136+556G=
ENST00000681049.1:n.50+1861G=
ENST00000681634.1:n.136+556G=
ENST00000245414.8:c.*145G=	ENSP00000245414.4:n.*145G=
ENST00000405885.6:c.*145G=	ENSP00000384406.1:n.*145G=
ENST00000472045.1:n.4432G=
NM_002198.2:c.*145G=	NP_002189.1:n.*145G=
XM_011543378.1:c.*145G=	XP_011541680.1:n.*145G=
XM_011543379.1:c.*145G=	XP_011541681.1:n.*145G=
XR_427711.2:n.1184G=
NM_001354924.1:c.*145G=	NP_001341853.1:n.*145G=
NM_001354925.1:c.*145G=	NP_001341854.1:n.*145G=
NR_149068.1:n.1184G=
XM_011543379.2:c.*145G=	XP_011541681.1:n.*145G=
NM_002198.3:c.*145G= MANE Select	NP_002189.1:n.*145G=