Canonical Allele Identifier: CA1583185148
Gene: IRF1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.132484117G= , CM000667.2:g.132484117G= GRCh38
NC_000005.9:g.131819809G= , CM000667.1:g.131819809G= GRCh37
NC_000005.8:g.131847708G= NCBI36
NG_011450.1:g.11657C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000245414.9:c.854-42C= MANE Select ENSP00000245414.4:n.854-42C=
ENST00000613424.5:c.*75-42C= ENSP00000480887.1:n.*75-42C=
ENST00000638452.2:c.-169+34428G= ENSP00000492349.2:n.-169+34428G=
ENST00000638504.1:n.206+64177G=
ENST00000638568.2:c.-311+34428G= ENSP00000491158.2:n.-311+34428G=
ENST00000639899.1:n.289+34428G=
ENST00000640655.2:c.-637-2075G= ENSP00000491596.2:n.-637-2075G=
ENST00000679743.1:c.475-42C= ENSP00000505257.1:n.475-42C=
ENST00000679786.1:n.130+2440C=
ENST00000679860.1:c.142-42C=
ENST00000679921.1:c.292+2440C= ENSP00000505766.1:n.292+2440C=
ENST00000679945.1:n.130+2440C=
ENST00000679964.1:n.50+1550C=
ENST00000680139.1:c.668-42C= ENSP00000506148.1:n.668-42C=
ENST00000680380.1:n.136+245C=
ENST00000680562.1:c.302-42C= ENSP00000505853.1:n.302-42C=
ENST00000680594.1:n.136+245C=
ENST00000680903.1:c.731-42C= ENSP00000505720.1:n.731-42C=
ENST00000681049.1:n.50+1550C=
ENST00000681240.1:c.104-42C= ENSP00000506034.1:n.104-42C=
ENST00000681336.1:c.137-78C= ENSP00000505242.1:n.137-78C=
ENST00000681462.1:c.691-42C=
ENST00000681595.1:c.415-42C= ENSP00000506023.1:n.415-42C=
ENST00000681634.1:n.136+245C=
ENST00000681694.1:c.166-42C= ENSP00000506552.1:n.166-42C=
ENST00000681715.1:c.352-42C= ENSP00000506545.1:n.352-42C=
ENST00000245414.8:c.854-42C= ENSP00000245414.4:n.854-42C=
ENST00000405885.6:c.854-42C= ENSP00000384406.1:n.854-42C=
ENST00000472045.1:n.4121C=
ENST00000613424.4:c.*75-42C= ENSP00000480887.1:n.*75-42C=
NM_002198.2:c.854-42C= NP_002189.1:n.854-42C=
XM_011543378.1:c.731-42C= XP_011541680.1:n.731-42C=
XM_011543379.1:c.602-42C= XP_011541681.1:n.602-42C=
XR_427711.2:n.915-42C=
NM_001354924.1:c.731-42C= NP_001341853.1:n.731-42C=
NM_001354925.1:c.668-42C= NP_001341854.1:n.668-42C=
NR_149068.1:n.915-42C=
XM_011543379.2:c.602-42C= XP_011541681.1:n.602-42C=
NM_002198.3:c.854-42C= MANE Select NP_002189.1:n.854-42C=