Canonical Allele Identifier: CA1583185113
Gene: IRF1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.132484030T= , CM000667.2:g.132484030T= GRCh38
NC_000005.9:g.131819722T= , CM000667.1:g.131819722T= GRCh37
NC_000005.8:g.131847621T= NCBI36
NG_011450.1:g.11744A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000245414.9:c.899A= MANE Select ENSP00000245414.4:p.Asn300=
ENST00000638452.2:c.-169+34341T= ENSP00000492349.2:n.-169+34341T=
ENST00000638504.1:n.206+64090T=
ENST00000638568.2:c.-311+34341T= ENSP00000491158.2:n.-311+34341T=
ENST00000639899.1:n.289+34341T=
ENST00000640655.2:c.-637-2162T= ENSP00000491596.2:n.-637-2162T=
ENST00000679743.1:c.520A= ENSP00000505257.1:n.520A=
ENST00000679786.1:n.130+2527A=
ENST00000679860.1:c.187A=
ENST00000679921.1:c.292+2527A= ENSP00000505766.1:n.292+2527A=
ENST00000679945.1:n.130+2527A=
ENST00000679964.1:n.50+1637A=
ENST00000680139.1:c.713A= ENSP00000506148.1:p.Asn238=
ENST00000680380.1:n.136+332A=
ENST00000680562.1:c.347A= ENSP00000505853.1:p.Asn116=
ENST00000680594.1:n.136+332A=
ENST00000680903.1:c.776A= ENSP00000505720.1:p.Asn259=
ENST00000681049.1:n.50+1637A=
ENST00000681240.1:c.149A= ENSP00000506034.1:p.Asn50=
ENST00000681336.1:c.146A= ENSP00000505242.1:p.Asn49=
ENST00000681462.1:c.736A=
ENST00000681595.1:c.460A= ENSP00000506023.1:n.460A=
ENST00000681634.1:n.136+332A=
ENST00000681694.1:c.211A= ENSP00000506552.1:n.211A=
ENST00000681715.1:c.397A= ENSP00000506545.1:n.397A=
ENST00000245414.8:c.899A= ENSP00000245414.4:p.Asn300=
ENST00000405885.6:c.899A= ENSP00000384406.1:p.Asn300=
ENST00000472045.1:n.4208A=
NM_002198.2:c.899A= NP_002189.1:p.Asn300=
XM_011543378.1:c.776A= XP_011541680.1:p.Asn259=
XM_011543379.1:c.647A= XP_011541681.1:p.Asn216=
XR_427711.2:n.960A=
NM_001354924.1:c.776A= NP_001341853.1:p.Asn259=
NM_001354925.1:c.713A= NP_001341854.1:p.Asn238=
NR_149068.1:n.960A=
XM_011543379.2:c.647A= XP_011541681.1:p.Asn216=
NM_002198.3:c.899A= MANE Select NP_002189.1:p.Asn300=