Canonical Allele Identifier: CA446358617

Gene: IRF1

Linked Data

• MyVariant Identifiers: chr5:g.131819750G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132484058G>A , CM000667.2:g.132484058G>A	GRCh38
NC_000005.9:g.131819750G>A , CM000667.1:g.131819750G>A	GRCh37
NC_000005.8:g.131847649G>A	NCBI36
NG_011450.1:g.11716C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000245414.9:c.871C>T MANE Select	ENSP00000245414.4:p.Leu291=
ENST00000613424.5:c.*92C>T	ENSP00000480887.1:n.*92C>T
ENST00000638452.2:c.-169+34369G>A	ENSP00000492349.2:n.-169+34369G>A
ENST00000638504.1:n.206+64118G>A
ENST00000638568.2:c.-311+34369G>A	ENSP00000491158.2:n.-311+34369G>A
ENST00000639899.1:n.289+34369G>A
ENST00000640655.2:c.-637-2134G>A	ENSP00000491596.2:n.-637-2134G>A
ENST00000679743.1:c.492C>T	ENSP00000505257.1:n.492C>T
ENST00000679786.1:n.130+2499C>T
ENST00000679860.1:c.159C>T
ENST00000679921.1:c.292+2499C>T	ENSP00000505766.1:n.292+2499C>T
ENST00000679945.1:n.130+2499C>T
ENST00000679964.1:n.50+1609C>T
ENST00000680139.1:c.685C>T	ENSP00000506148.1:p.Leu229=
ENST00000680380.1:n.136+304C>T
ENST00000680562.1:c.319C>T	ENSP00000505853.1:p.Leu107=
ENST00000680594.1:n.136+304C>T
ENST00000680903.1:c.748C>T	ENSP00000505720.1:p.Leu250=
ENST00000681049.1:n.50+1609C>T
ENST00000681240.1:c.121C>T	ENSP00000506034.1:p.Leu41=
ENST00000681336.1:c.137-19C>T	ENSP00000505242.1:n.137-19C>T
ENST00000681462.1:c.708C>T
ENST00000681595.1:c.432C>T	ENSP00000506023.1:n.432C>T
ENST00000681634.1:n.136+304C>T
ENST00000681694.1:c.183C>T	ENSP00000506552.1:n.183C>T
ENST00000681715.1:c.369C>T	ENSP00000506545.1:n.369C>T
ENST00000245414.8:c.871C>T	ENSP00000245414.4:p.Leu291=
ENST00000405885.6:c.871C>T	ENSP00000384406.1:p.Leu291=
ENST00000472045.1:n.4180C>T
ENST00000613424.4:c.*92C>T	ENSP00000480887.1:n.*92C>T
NM_002198.2:c.871C>T	NP_002189.1:p.Leu291=
XM_011543378.1:c.748C>T	XP_011541680.1:p.Leu250=
XM_011543379.1:c.619C>T	XP_011541681.1:p.Leu207=
XR_427711.2:n.932C>T
NM_001354924.1:c.748C>T	NP_001341853.1:p.Leu250=
NM_001354925.1:c.685C>T	NP_001341854.1:p.Leu229=
NR_149068.1:n.932C>T
XM_011543379.2:c.619C>T	XP_011541681.1:p.Leu207=
NM_002198.3:c.871C>T MANE Select	NP_002189.1:p.Leu291=