Canonical Allele Identifier: CA1583185152

Gene: IRF1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132484126T= , CM000667.2:g.132484126T=	GRCh38
NC_000005.9:g.131819818T= , CM000667.1:g.131819818T=	GRCh37
NC_000005.8:g.131847717T=	NCBI36
NG_011450.1:g.11648A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000245414.9:c.854-51A= MANE Select	ENSP00000245414.4:n.854-51A=
ENST00000613424.5:c.*75-51A=	ENSP00000480887.1:n.*75-51A=
ENST00000638452.2:c.-169+34437T=	ENSP00000492349.2:n.-169+34437T=
ENST00000638504.1:n.206+64186T=
ENST00000638568.2:c.-311+34437T=	ENSP00000491158.2:n.-311+34437T=
ENST00000639899.1:n.289+34437T=
ENST00000640655.2:c.-637-2066T=	ENSP00000491596.2:n.-637-2066T=
ENST00000679743.1:c.475-51A=	ENSP00000505257.1:n.475-51A=
ENST00000679786.1:n.130+2431A=
ENST00000679860.1:c.142-51A=
ENST00000679921.1:c.292+2431A=	ENSP00000505766.1:n.292+2431A=
ENST00000679945.1:n.130+2431A=
ENST00000679964.1:n.50+1541A=
ENST00000680139.1:c.668-51A=	ENSP00000506148.1:n.668-51A=
ENST00000680380.1:n.136+236A=
ENST00000680562.1:c.302-51A=	ENSP00000505853.1:n.302-51A=
ENST00000680594.1:n.136+236A=
ENST00000680903.1:c.731-51A=	ENSP00000505720.1:n.731-51A=
ENST00000681049.1:n.50+1541A=
ENST00000681240.1:c.104-51A=	ENSP00000506034.1:n.104-51A=
ENST00000681336.1:c.137-87A=	ENSP00000505242.1:n.137-87A=
ENST00000681462.1:c.691-51A=
ENST00000681595.1:c.415-51A=	ENSP00000506023.1:n.415-51A=
ENST00000681634.1:n.136+236A=
ENST00000681694.1:c.166-51A=	ENSP00000506552.1:n.166-51A=
ENST00000681715.1:c.352-51A=	ENSP00000506545.1:n.352-51A=
ENST00000245414.8:c.854-51A=	ENSP00000245414.4:n.854-51A=
ENST00000405885.6:c.854-51A=	ENSP00000384406.1:n.854-51A=
ENST00000472045.1:n.4112A=
ENST00000613424.4:c.*75-51A=	ENSP00000480887.1:n.*75-51A=
NM_002198.2:c.854-51A=	NP_002189.1:n.854-51A=
XM_011543378.1:c.731-51A=	XP_011541680.1:n.731-51A=
XM_011543379.1:c.602-51A=	XP_011541681.1:n.602-51A=
XR_427711.2:n.915-51A=
NM_001354924.1:c.731-51A=	NP_001341853.1:n.731-51A=
NM_001354925.1:c.668-51A=	NP_001341854.1:n.668-51A=
NR_149068.1:n.915-51A=
XM_011543379.2:c.602-51A=	XP_011541681.1:n.602-51A=
NM_002198.3:c.854-51A= MANE Select	NP_002189.1:n.854-51A=