Canonical Allele Identifier: CA360813845

Gene: IRF1

Linked Data

• MyVariant Identifiers: chr5:g.131819672A>T (hg19) ; chr5:g.132483980A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132483980A>T , CM000667.2:g.132483980A>T	GRCh38
NC_000005.9:g.131819672A>T , CM000667.1:g.131819672A>T	GRCh37
NC_000005.8:g.131847571A>T	NCBI36
NG_011450.1:g.11794T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000245414.9:c.949T>A MANE Select	ENSP00000245414.4:p.Ser317Thr
ENST00000638452.2:c.-169+34291A>T	ENSP00000492349.2:n.-169+34291A>T
ENST00000638504.1:n.206+64040A>T
ENST00000638568.2:c.-311+34291A>T	ENSP00000491158.2:n.-311+34291A>T
ENST00000639899.1:n.289+34291A>T
ENST00000640655.2:c.-637-2212A>T	ENSP00000491596.2:n.-637-2212A>T
ENST00000679743.1:c.570T>A	ENSP00000505257.1:n.570T>A
ENST00000679786.1:n.130+2577T>A
ENST00000679860.1:c.237T>A
ENST00000679921.1:c.292+2577T>A	ENSP00000505766.1:n.292+2577T>A
ENST00000679945.1:n.130+2577T>A
ENST00000679964.1:n.50+1687T>A
ENST00000680139.1:c.763T>A	ENSP00000506148.1:p.Ser255Thr
ENST00000680380.1:n.136+382T>A
ENST00000680562.1:c.397T>A	ENSP00000505853.1:p.Ser133Thr
ENST00000680594.1:n.136+382T>A
ENST00000680903.1:c.826T>A	ENSP00000505720.1:p.Ser276Thr
ENST00000681049.1:n.50+1687T>A
ENST00000681240.1:c.199T>A	ENSP00000506034.1:p.Ser67Thr
ENST00000681336.1:c.196T>A	ENSP00000505242.1:p.Ser66Thr
ENST00000681462.1:c.786T>A
ENST00000681595.1:c.510T>A	ENSP00000506023.1:n.510T>A
ENST00000681634.1:n.136+382T>A
ENST00000681694.1:c.261T>A	ENSP00000506552.1:n.261T>A
ENST00000681715.1:c.447T>A	ENSP00000506545.1:n.447T>A
ENST00000245414.8:c.949T>A	ENSP00000245414.4:p.Ser317Thr
ENST00000405885.6:c.949T>A	ENSP00000384406.1:p.Ser317Thr
ENST00000472045.1:n.4258T>A
NM_002198.2:c.949T>A	NP_002189.1:p.Ser317Thr
XM_011543378.1:c.826T>A	XP_011541680.1:p.Ser276Thr
XM_011543379.1:c.697T>A	XP_011541681.1:p.Ser233Thr
XR_427711.2:n.1010T>A
NM_001354924.1:c.826T>A	NP_001341853.1:p.Ser276Thr
NM_001354925.1:c.763T>A	NP_001341854.1:p.Ser255Thr
NR_149068.1:n.1010T>A
XM_011543379.2:c.697T>A	XP_011541681.1:p.Ser233Thr
NM_002198.3:c.949T>A MANE Select	NP_002189.1:p.Ser317Thr