Canonical Allele Identifier: CA360814035
Gene: IRF1 HGNC NCBI

Linked Data

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid Change
ENST00000245414.9:c.859A>C MANE Select ENSP00000245414.4:p.Ile287Leu
ENST00000613424.5:c.*80A>C ENSP00000480887.1:n.*80A>C
ENST00000638452.2:c.-169+34381T>G ENSP00000492349.2:n.-169+34381T>G
ENST00000638504.1:n.206+64130T>G
ENST00000638568.2:c.-311+34381T>G ENSP00000491158.2:n.-311+34381T>G
ENST00000639899.1:n.289+34381T>G
ENST00000640655.2:c.-637-2122T>G ENSP00000491596.2:n.-637-2122T>G
ENST00000679743.1:c.480A>C ENSP00000505257.1:n.480A>C
ENST00000679786.1:n.130+2487A>C
ENST00000679860.1:c.147A>C
ENST00000679921.1:c.292+2487A>C ENSP00000505766.1:n.292+2487A>C
ENST00000679945.1:n.130+2487A>C
ENST00000679964.1:n.50+1597A>C
ENST00000680139.1:c.673A>C ENSP00000506148.1:p.Ile225Leu
ENST00000680380.1:n.136+292A>C
ENST00000680562.1:c.307A>C ENSP00000505853.1:p.Ile103Leu
ENST00000680594.1:n.136+292A>C
ENST00000680903.1:c.736A>C ENSP00000505720.1:p.Ile246Leu
ENST00000681049.1:n.50+1597A>C
ENST00000681240.1:c.109A>C ENSP00000506034.1:p.Ile37Leu
ENST00000681336.1:c.137-31A>C ENSP00000505242.1:n.137-31A>C
ENST00000681462.1:c.696A>C
ENST00000681595.1:c.420A>C ENSP00000506023.1:n.420A>C
ENST00000681634.1:n.136+292A>C
ENST00000681694.1:c.171A>C ENSP00000506552.1:p.Ile57=
ENST00000681715.1:c.357A>C ENSP00000506545.1:n.357A>C
ENST00000245414.8:c.859A>C ENSP00000245414.4:p.Ile287Leu
ENST00000405885.6:c.859A>C ENSP00000384406.1:p.Ile287Leu
ENST00000472045.1:n.4168A>C
ENST00000613424.4:c.*80A>C ENSP00000480887.1:n.*80A>C
NM_002198.2:c.859A>C NP_002189.1:p.Ile287Leu
XM_011543378.1:c.736A>C XP_011541680.1:p.Ile246Leu
XM_011543379.1:c.607A>C XP_011541681.1:p.Ile203Leu
XR_427711.2:n.920A>C
NM_001354924.1:c.736A>C NP_001341853.1:p.Ile246Leu
NM_001354925.1:c.673A>C NP_001341854.1:p.Ile225Leu
NR_149068.1:n.920A>C
XM_011543379.2:c.607A>C XP_011541681.1:p.Ile203Leu
NM_002198.3:c.859A>C MANE Select NP_002189.1:p.Ile287Leu