Canonical Allele Identifier: CA1583184990
Gene: IRF1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.132483677T= , CM000667.2:g.132483677T= GRCh38
NC_000005.9:g.131819369T= , CM000667.1:g.131819369T= GRCh37
NC_000005.8:g.131847268T= NCBI36
NG_011450.1:g.12097A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000245414.9:c.*274A= MANE Select ENSP00000245414.4:n.*274A=
ENST00000638452.2:c.-169+33988T= ENSP00000492349.2:n.-169+33988T=
ENST00000638504.1:n.206+63737T=
ENST00000638568.2:c.-311+33988T= ENSP00000491158.2:n.-311+33988T=
ENST00000639899.1:n.289+33988T=
ENST00000640655.2:c.-637-2515T= ENSP00000491596.2:n.-637-2515T=
ENST00000679786.1:n.130+2880A=
ENST00000679921.1:c.292+2880A= ENSP00000505766.1:n.292+2880A=
ENST00000679945.1:n.130+2880A=
ENST00000679964.1:n.50+1990A=
ENST00000680380.1:n.136+685A=
ENST00000680594.1:n.136+685A=
ENST00000681049.1:n.50+1990A=
ENST00000681634.1:n.136+685A=
ENST00000245414.8:c.*274A= ENSP00000245414.4:n.*274A=
ENST00000405885.6:c.*274A= ENSP00000384406.1:n.*274A=
ENST00000472045.1:n.4561A=
NM_002198.2:c.*274A= NP_002189.1:n.*274A=
XM_011543378.1:c.*274A= XP_011541680.1:n.*274A=
XM_011543379.1:c.*274A= XP_011541681.1:n.*274A=
XR_427711.2:n.1313A=
NM_001354924.1:c.*274A= NP_001341853.1:n.*274A=
NM_001354925.1:c.*274A= NP_001341854.1:n.*274A=
NR_149068.1:n.1313A=
XM_011543379.2:c.*274A= XP_011541681.1:n.*274A=
NM_002198.3:c.*274A= MANE Select NP_002189.1:n.*274A=