Canonical Allele Identifier: CA1583185125
Gene: IRF1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.132484070T= , CM000667.2:g.132484070T= GRCh38
NC_000005.9:g.131819762T= , CM000667.1:g.131819762T= GRCh37
NC_000005.8:g.131847661T= NCBI36
NG_011450.1:g.11704A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000245414.9:c.859A= MANE Select ENSP00000245414.4:p.Ile287=
ENST00000613424.5:c.*80A= ENSP00000480887.1:n.*80A=
ENST00000638452.2:c.-169+34381T= ENSP00000492349.2:n.-169+34381T=
ENST00000638504.1:n.206+64130T=
ENST00000638568.2:c.-311+34381T= ENSP00000491158.2:n.-311+34381T=
ENST00000639899.1:n.289+34381T=
ENST00000640655.2:c.-637-2122T= ENSP00000491596.2:n.-637-2122T=
ENST00000679743.1:c.480A= ENSP00000505257.1:n.480A=
ENST00000679786.1:n.130+2487A=
ENST00000679860.1:c.147A=
ENST00000679921.1:c.292+2487A= ENSP00000505766.1:n.292+2487A=
ENST00000679945.1:n.130+2487A=
ENST00000679964.1:n.50+1597A=
ENST00000680139.1:c.673A= ENSP00000506148.1:p.Ile225=
ENST00000680380.1:n.136+292A=
ENST00000680562.1:c.307A= ENSP00000505853.1:p.Ile103=
ENST00000680594.1:n.136+292A=
ENST00000680903.1:c.736A= ENSP00000505720.1:p.Ile246=
ENST00000681049.1:n.50+1597A=
ENST00000681240.1:c.109A= ENSP00000506034.1:p.Ile37=
ENST00000681336.1:c.137-31A= ENSP00000505242.1:n.137-31A=
ENST00000681462.1:c.696A=
ENST00000681595.1:c.420A= ENSP00000506023.1:n.420A=
ENST00000681634.1:n.136+292A=
ENST00000681694.1:c.171A= ENSP00000506552.1:p.Ile57=
ENST00000681715.1:c.357A= ENSP00000506545.1:n.357A=
ENST00000245414.8:c.859A= ENSP00000245414.4:p.Ile287=
ENST00000405885.6:c.859A= ENSP00000384406.1:p.Ile287=
ENST00000472045.1:n.4168A=
ENST00000613424.4:c.*80A= ENSP00000480887.1:n.*80A=
NM_002198.2:c.859A= NP_002189.1:p.Ile287=
XM_011543378.1:c.736A= XP_011541680.1:p.Ile246=
XM_011543379.1:c.607A= XP_011541681.1:p.Ile203=
XR_427711.2:n.920A=
NM_001354924.1:c.736A= NP_001341853.1:p.Ile246=
NM_001354925.1:c.673A= NP_001341854.1:p.Ile225=
NR_149068.1:n.920A=
XM_011543379.2:c.607A= XP_011541681.1:p.Ile203=
NM_002198.3:c.859A= MANE Select NP_002189.1:p.Ile287=