Canonical Allele Identifier: CA360814032

Gene: IRF1

Linked Data

• MyVariant Identifiers: chr5:g.131819761A>T (hg19) ; chr5:g.132484069A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132484069A>T , CM000667.2:g.132484069A>T	GRCh38
NC_000005.9:g.131819761A>T , CM000667.1:g.131819761A>T	GRCh37
NC_000005.8:g.131847660A>T	NCBI36
NG_011450.1:g.11705T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000245414.9:c.860T>A MANE Select	ENSP00000245414.4:p.Ile287Asn
ENST00000613424.5:c.*81T>A	ENSP00000480887.1:n.*81T>A
ENST00000638452.2:c.-169+34380A>T	ENSP00000492349.2:n.-169+34380A>T
ENST00000638504.1:n.206+64129A>T
ENST00000638568.2:c.-311+34380A>T	ENSP00000491158.2:n.-311+34380A>T
ENST00000639899.1:n.289+34380A>T
ENST00000640655.2:c.-637-2123A>T	ENSP00000491596.2:n.-637-2123A>T
ENST00000679743.1:c.481T>A	ENSP00000505257.1:n.481T>A
ENST00000679786.1:n.130+2488T>A
ENST00000679860.1:c.148T>A
ENST00000679921.1:c.292+2488T>A	ENSP00000505766.1:n.292+2488T>A
ENST00000679945.1:n.130+2488T>A
ENST00000679964.1:n.50+1598T>A
ENST00000680139.1:c.674T>A	ENSP00000506148.1:p.Ile225Asn
ENST00000680380.1:n.136+293T>A
ENST00000680562.1:c.308T>A	ENSP00000505853.1:p.Ile103Asn
ENST00000680594.1:n.136+293T>A
ENST00000680903.1:c.737T>A	ENSP00000505720.1:p.Ile246Asn
ENST00000681049.1:n.50+1598T>A
ENST00000681240.1:c.110T>A	ENSP00000506034.1:p.Ile37Asn
ENST00000681336.1:c.137-30T>A	ENSP00000505242.1:n.137-30T>A
ENST00000681462.1:c.697T>A
ENST00000681595.1:c.421T>A	ENSP00000506023.1:n.421T>A
ENST00000681634.1:n.136+293T>A
ENST00000681694.1:c.172T>A	ENSP00000506552.1:p.Leu58Met
ENST00000681715.1:c.358T>A	ENSP00000506545.1:n.358T>A
ENST00000245414.8:c.860T>A	ENSP00000245414.4:p.Ile287Asn
ENST00000405885.6:c.860T>A	ENSP00000384406.1:p.Ile287Asn
ENST00000472045.1:n.4169T>A
ENST00000613424.4:c.*81T>A	ENSP00000480887.1:n.*81T>A
NM_002198.2:c.860T>A	NP_002189.1:p.Ile287Asn
XM_011543378.1:c.737T>A	XP_011541680.1:p.Ile246Asn
XM_011543379.1:c.608T>A	XP_011541681.1:p.Ile203Asn
XR_427711.2:n.921T>A
NM_001354924.1:c.737T>A	NP_001341853.1:p.Ile246Asn
NM_001354925.1:c.674T>A	NP_001341854.1:p.Ile225Asn
NR_149068.1:n.921T>A
XM_011543379.2:c.608T>A	XP_011541681.1:p.Ile203Asn
NM_002198.3:c.860T>A MANE Select	NP_002189.1:p.Ile287Asn