Canonical Allele Identifier: CA1583185120
Gene: IRF1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.132484049C= , CM000667.2:g.132484049C= GRCh38
NC_000005.9:g.131819741C= , CM000667.1:g.131819741C= GRCh37
NC_000005.8:g.131847640C= NCBI36
NG_011450.1:g.11725G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000245414.9:c.880G= MANE Select ENSP00000245414.4:p.Val294=
ENST00000638452.2:c.-169+34360C= ENSP00000492349.2:n.-169+34360C=
ENST00000638504.1:n.206+64109C=
ENST00000638568.2:c.-311+34360C= ENSP00000491158.2:n.-311+34360C=
ENST00000639899.1:n.289+34360C=
ENST00000640655.2:c.-637-2143C= ENSP00000491596.2:n.-637-2143C=
ENST00000679743.1:c.501G= ENSP00000505257.1:n.501G=
ENST00000679786.1:n.130+2508G=
ENST00000679860.1:c.168G=
ENST00000679921.1:c.292+2508G= ENSP00000505766.1:n.292+2508G=
ENST00000679945.1:n.130+2508G=
ENST00000679964.1:n.50+1618G=
ENST00000680139.1:c.694G= ENSP00000506148.1:p.Val232=
ENST00000680380.1:n.136+313G=
ENST00000680562.1:c.328G= ENSP00000505853.1:p.Val110=
ENST00000680594.1:n.136+313G=
ENST00000680903.1:c.757G= ENSP00000505720.1:p.Val253=
ENST00000681049.1:n.50+1618G=
ENST00000681240.1:c.130G= ENSP00000506034.1:p.Val44=
ENST00000681336.1:c.137-10G= ENSP00000505242.1:n.137-10G=
ENST00000681462.1:c.717G=
ENST00000681595.1:c.441G= ENSP00000506023.1:n.441G=
ENST00000681634.1:n.136+313G=
ENST00000681694.1:c.192G= ENSP00000506552.1:n.192G=
ENST00000681715.1:c.378G= ENSP00000506545.1:n.378G=
ENST00000245414.8:c.880G= ENSP00000245414.4:p.Val294=
ENST00000405885.6:c.880G= ENSP00000384406.1:p.Val294=
ENST00000472045.1:n.4189G=
NM_002198.2:c.880G= NP_002189.1:p.Val294=
XM_011543378.1:c.757G= XP_011541680.1:p.Val253=
XM_011543379.1:c.628G= XP_011541681.1:p.Val210=
XR_427711.2:n.941G=
NM_001354924.1:c.757G= NP_001341853.1:p.Val253=
NM_001354925.1:c.694G= NP_001341854.1:p.Val232=
NR_149068.1:n.941G=
XM_011543379.2:c.628G= XP_011541681.1:p.Val210=
NM_002198.3:c.880G= MANE Select NP_002189.1:p.Val294=