Canonical Allele Identifier: CA1583185122
Gene: IRF1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.132484052G= , CM000667.2:g.132484052G= GRCh38
NC_000005.9:g.131819744G= , CM000667.1:g.131819744G= GRCh37
NC_000005.8:g.131847643G= NCBI36
NG_011450.1:g.11722C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000245414.9:c.877C= MANE Select ENSP00000245414.4:p.Arg293=
ENST00000613424.5:c.*98C= ENSP00000480887.1:n.*98C=
ENST00000638452.2:c.-169+34363G= ENSP00000492349.2:n.-169+34363G=
ENST00000638504.1:n.206+64112G=
ENST00000638568.2:c.-311+34363G= ENSP00000491158.2:n.-311+34363G=
ENST00000639899.1:n.289+34363G=
ENST00000640655.2:c.-637-2140G= ENSP00000491596.2:n.-637-2140G=
ENST00000679743.1:c.498C= ENSP00000505257.1:n.498C=
ENST00000679786.1:n.130+2505C=
ENST00000679860.1:c.165C=
ENST00000679921.1:c.292+2505C= ENSP00000505766.1:n.292+2505C=
ENST00000679945.1:n.130+2505C=
ENST00000679964.1:n.50+1615C=
ENST00000680139.1:c.691C= ENSP00000506148.1:p.Arg231=
ENST00000680380.1:n.136+310C=
ENST00000680562.1:c.325C= ENSP00000505853.1:p.Arg109=
ENST00000680594.1:n.136+310C=
ENST00000680903.1:c.754C= ENSP00000505720.1:p.Arg252=
ENST00000681049.1:n.50+1615C=
ENST00000681240.1:c.127C= ENSP00000506034.1:p.Arg43=
ENST00000681336.1:c.137-13C= ENSP00000505242.1:n.137-13C=
ENST00000681462.1:c.714C=
ENST00000681595.1:c.438C= ENSP00000506023.1:n.438C=
ENST00000681634.1:n.136+310C=
ENST00000681694.1:c.189C= ENSP00000506552.1:n.189C=
ENST00000681715.1:c.375C= ENSP00000506545.1:n.375C=
ENST00000245414.8:c.877C= ENSP00000245414.4:p.Arg293=
ENST00000405885.6:c.877C= ENSP00000384406.1:p.Arg293=
ENST00000472045.1:n.4186C=
ENST00000613424.4:c.*98C= ENSP00000480887.1:n.*98C=
NM_002198.2:c.877C= NP_002189.1:p.Arg293=
XM_011543378.1:c.754C= XP_011541680.1:p.Arg252=
XM_011543379.1:c.625C= XP_011541681.1:p.Arg209=
XR_427711.2:n.938C=
NM_001354924.1:c.754C= NP_001341853.1:p.Arg252=
NM_001354925.1:c.691C= NP_001341854.1:p.Arg231=
NR_149068.1:n.938C=
XM_011543379.2:c.625C= XP_011541681.1:p.Arg209=
NM_002198.3:c.877C= MANE Select NP_002189.1:p.Arg293=