Canonical Allele Identifier: CA360813904

Gene: IRF1

Linked Data

• MyVariant Identifiers: chr5:g.131819702C>A (hg19) ; chr5:g.132484010C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132484010C>A , CM000667.2:g.132484010C>A	GRCh38
NC_000005.9:g.131819702C>A , CM000667.1:g.131819702C>A	GRCh37
NC_000005.8:g.131847601C>A	NCBI36
NG_011450.1:g.11764G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000245414.9:c.919G>T MANE Select	ENSP00000245414.4:p.Asp307Tyr
ENST00000638452.2:c.-169+34321C>A	ENSP00000492349.2:n.-169+34321C>A
ENST00000638504.1:n.206+64070C>A
ENST00000638568.2:c.-311+34321C>A	ENSP00000491158.2:n.-311+34321C>A
ENST00000639899.1:n.289+34321C>A
ENST00000640655.2:c.-637-2182C>A	ENSP00000491596.2:n.-637-2182C>A
ENST00000679743.1:c.540G>T	ENSP00000505257.1:n.540G>T
ENST00000679786.1:n.130+2547G>T
ENST00000679860.1:c.207G>T
ENST00000679921.1:c.292+2547G>T	ENSP00000505766.1:n.292+2547G>T
ENST00000679945.1:n.130+2547G>T
ENST00000679964.1:n.50+1657G>T
ENST00000680139.1:c.733G>T	ENSP00000506148.1:p.Asp245Tyr
ENST00000680380.1:n.136+352G>T
ENST00000680562.1:c.367G>T	ENSP00000505853.1:p.Asp123Tyr
ENST00000680594.1:n.136+352G>T
ENST00000680903.1:c.796G>T	ENSP00000505720.1:p.Asp266Tyr
ENST00000681049.1:n.50+1657G>T
ENST00000681240.1:c.169G>T	ENSP00000506034.1:p.Asp57Tyr
ENST00000681336.1:c.166G>T	ENSP00000505242.1:p.Asp56Tyr
ENST00000681462.1:c.756G>T
ENST00000681595.1:c.480G>T	ENSP00000506023.1:n.480G>T
ENST00000681634.1:n.136+352G>T
ENST00000681694.1:c.231G>T	ENSP00000506552.1:n.231G>T
ENST00000681715.1:c.417G>T	ENSP00000506545.1:n.417G>T
ENST00000245414.8:c.919G>T	ENSP00000245414.4:p.Asp307Tyr
ENST00000405885.6:c.919G>T	ENSP00000384406.1:p.Asp307Tyr
ENST00000472045.1:n.4228G>T
NM_002198.2:c.919G>T	NP_002189.1:p.Asp307Tyr
XM_011543378.1:c.796G>T	XP_011541680.1:p.Asp266Tyr
XM_011543379.1:c.667G>T	XP_011541681.1:p.Asp223Tyr
XR_427711.2:n.980G>T
NM_001354924.1:c.796G>T	NP_001341853.1:p.Asp266Tyr
NM_001354925.1:c.733G>T	NP_001341854.1:p.Asp245Tyr
NR_149068.1:n.980G>T
XM_011543379.2:c.667G>T	XP_011541681.1:p.Asp223Tyr
NM_002198.3:c.919G>T MANE Select	NP_002189.1:p.Asp307Tyr