Canonical Allele Identifier: CA1583185098
Gene: IRF1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.132483989G= , CM000667.2:g.132483989G= GRCh38
NC_000005.9:g.131819681G= , CM000667.1:g.131819681G= GRCh37
NC_000005.8:g.131847580G= NCBI36
NG_011450.1:g.11785C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000245414.9:c.940C= MANE Select ENSP00000245414.4:p.Arg314=
ENST00000638452.2:c.-169+34300G= ENSP00000492349.2:n.-169+34300G=
ENST00000638504.1:n.206+64049G=
ENST00000638568.2:c.-311+34300G= ENSP00000491158.2:n.-311+34300G=
ENST00000639899.1:n.289+34300G=
ENST00000640655.2:c.-637-2203G= ENSP00000491596.2:n.-637-2203G=
ENST00000679743.1:c.561C= ENSP00000505257.1:n.561C=
ENST00000679786.1:n.130+2568C=
ENST00000679860.1:c.228C=
ENST00000679921.1:c.292+2568C= ENSP00000505766.1:n.292+2568C=
ENST00000679945.1:n.130+2568C=
ENST00000679964.1:n.50+1678C=
ENST00000680139.1:c.754C= ENSP00000506148.1:p.Arg252=
ENST00000680380.1:n.136+373C=
ENST00000680562.1:c.388C= ENSP00000505853.1:p.Arg130=
ENST00000680594.1:n.136+373C=
ENST00000680903.1:c.817C= ENSP00000505720.1:p.Arg273=
ENST00000681049.1:n.50+1678C=
ENST00000681240.1:c.190C= ENSP00000506034.1:p.Arg64=
ENST00000681336.1:c.187C= ENSP00000505242.1:p.Arg63=
ENST00000681462.1:c.777C=
ENST00000681595.1:c.501C= ENSP00000506023.1:n.501C=
ENST00000681634.1:n.136+373C=
ENST00000681694.1:c.252C= ENSP00000506552.1:n.252C=
ENST00000681715.1:c.438C= ENSP00000506545.1:n.438C=
ENST00000245414.8:c.940C= ENSP00000245414.4:p.Arg314=
ENST00000405885.6:c.940C= ENSP00000384406.1:p.Arg314=
ENST00000472045.1:n.4249C=
NM_002198.2:c.940C= NP_002189.1:p.Arg314=
XM_011543378.1:c.817C= XP_011541680.1:p.Arg273=
XM_011543379.1:c.688C= XP_011541681.1:p.Arg230=
XR_427711.2:n.1001C=
NM_001354924.1:c.817C= NP_001341853.1:p.Arg273=
NM_001354925.1:c.754C= NP_001341854.1:p.Arg252=
NR_149068.1:n.1001C=
XM_011543379.2:c.688C= XP_011541681.1:p.Arg230=
NM_002198.3:c.940C= MANE Select NP_002189.1:p.Arg314=