Canonical Allele Identifier: CA360813998

Gene: IRF1

Linked Data

• MyVariant Identifiers: chr5:g.131819745C>A (hg19) ; chr5:g.132484053C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132484053C>A , CM000667.2:g.132484053C>A	GRCh38
NC_000005.9:g.131819745C>A , CM000667.1:g.131819745C>A	GRCh37
NC_000005.8:g.131847644C>A	NCBI36
NG_011450.1:g.11721G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000245414.9:c.876G>T MANE Select	ENSP00000245414.4:p.Gln292His
ENST00000613424.5:c.*97G>T	ENSP00000480887.1:n.*97G>T
ENST00000638452.2:c.-169+34364C>A	ENSP00000492349.2:n.-169+34364C>A
ENST00000638504.1:n.206+64113C>A
ENST00000638568.2:c.-311+34364C>A	ENSP00000491158.2:n.-311+34364C>A
ENST00000639899.1:n.289+34364C>A
ENST00000640655.2:c.-637-2139C>A	ENSP00000491596.2:n.-637-2139C>A
ENST00000679743.1:c.497G>T	ENSP00000505257.1:n.497G>T
ENST00000679786.1:n.130+2504G>T
ENST00000679860.1:c.164G>T
ENST00000679921.1:c.292+2504G>T	ENSP00000505766.1:n.292+2504G>T
ENST00000679945.1:n.130+2504G>T
ENST00000679964.1:n.50+1614G>T
ENST00000680139.1:c.690G>T	ENSP00000506148.1:p.Gln230His
ENST00000680380.1:n.136+309G>T
ENST00000680562.1:c.324G>T	ENSP00000505853.1:p.Gln108His
ENST00000680594.1:n.136+309G>T
ENST00000680903.1:c.753G>T	ENSP00000505720.1:p.Gln251His
ENST00000681049.1:n.50+1614G>T
ENST00000681240.1:c.126G>T	ENSP00000506034.1:p.Gln42His
ENST00000681336.1:c.137-14G>T	ENSP00000505242.1:n.137-14G>T
ENST00000681462.1:c.713G>T
ENST00000681595.1:c.437G>T	ENSP00000506023.1:n.437G>T
ENST00000681634.1:n.136+309G>T
ENST00000681694.1:c.188G>T	ENSP00000506552.1:n.188G>T
ENST00000681715.1:c.374G>T	ENSP00000506545.1:n.374G>T
ENST00000245414.8:c.876G>T	ENSP00000245414.4:p.Gln292His
ENST00000405885.6:c.876G>T	ENSP00000384406.1:p.Gln292His
ENST00000472045.1:n.4185G>T
ENST00000613424.4:c.*97G>T	ENSP00000480887.1:n.*97G>T
NM_002198.2:c.876G>T	NP_002189.1:p.Gln292His
XM_011543378.1:c.753G>T	XP_011541680.1:p.Gln251His
XM_011543379.1:c.624G>T	XP_011541681.1:p.Gln208His
XR_427711.2:n.937G>T
NM_001354924.1:c.753G>T	NP_001341853.1:p.Gln251His
NM_001354925.1:c.690G>T	NP_001341854.1:p.Gln230His
NR_149068.1:n.937G>T
XM_011543379.2:c.624G>T	XP_011541681.1:p.Gln208His
NM_002198.3:c.876G>T MANE Select	NP_002189.1:p.Gln292His