Canonical Allele Identifier: CA1583185109

Gene: IRF1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132484014C= , CM000667.2:g.132484014C=	GRCh38
NC_000005.9:g.131819706C= , CM000667.1:g.131819706C=	GRCh37
NC_000005.8:g.131847605C=	NCBI36
NG_011450.1:g.11760G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000245414.9:c.915G= MANE Select	ENSP00000245414.4:p.Trp305=
ENST00000638452.2:c.-169+34325C=	ENSP00000492349.2:n.-169+34325C=
ENST00000638504.1:n.206+64074C=
ENST00000638568.2:c.-311+34325C=	ENSP00000491158.2:n.-311+34325C=
ENST00000639899.1:n.289+34325C=
ENST00000640655.2:c.-637-2178C=	ENSP00000491596.2:n.-637-2178C=
ENST00000679743.1:c.536G=	ENSP00000505257.1:n.536G=
ENST00000679786.1:n.130+2543G=
ENST00000679860.1:c.203G=
ENST00000679921.1:c.292+2543G=	ENSP00000505766.1:n.292+2543G=
ENST00000679945.1:n.130+2543G=
ENST00000679964.1:n.50+1653G=
ENST00000680139.1:c.729G=	ENSP00000506148.1:p.Trp243=
ENST00000680380.1:n.136+348G=
ENST00000680562.1:c.363G=	ENSP00000505853.1:p.Trp121=
ENST00000680594.1:n.136+348G=
ENST00000680903.1:c.792G=	ENSP00000505720.1:p.Trp264=
ENST00000681049.1:n.50+1653G=
ENST00000681240.1:c.165G=	ENSP00000506034.1:p.Trp55=
ENST00000681336.1:c.162G=	ENSP00000505242.1:p.Trp54=
ENST00000681462.1:c.752G=
ENST00000681595.1:c.476G=	ENSP00000506023.1:n.476G=
ENST00000681634.1:n.136+348G=
ENST00000681694.1:c.227G=	ENSP00000506552.1:n.227G=
ENST00000681715.1:c.413G=	ENSP00000506545.1:n.413G=
ENST00000245414.8:c.915G=	ENSP00000245414.4:p.Trp305=
ENST00000405885.6:c.915G=	ENSP00000384406.1:p.Trp305=
ENST00000472045.1:n.4224G=
NM_002198.2:c.915G=	NP_002189.1:p.Trp305=
XM_011543378.1:c.792G=	XP_011541680.1:p.Trp264=
XM_011543379.1:c.663G=	XP_011541681.1:p.Trp221=
XR_427711.2:n.976G=
NM_001354924.1:c.792G=	NP_001341853.1:p.Trp264=
NM_001354925.1:c.729G=	NP_001341854.1:p.Trp243=
NR_149068.1:n.976G=
XM_011543379.2:c.663G=	XP_011541681.1:p.Trp221=
NM_002198.3:c.915G= MANE Select	NP_002189.1:p.Trp305=