Canonical Allele Identifier: CA360927877

Gene: IRF1

Linked Data

• MyVariant Identifiers: chr5:g.131825140A>T (hg19) ; chr5:g.132489448A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132489448A>T , CM000667.2:g.132489448A>T	GRCh38
NC_000005.9:g.131825140A>T , CM000667.1:g.131825140A>T	GRCh37
NC_000005.8:g.131853039A>T	NCBI36
NG_011450.1:g.6326T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000245414.9:c.31T>A MANE Select	ENSP00000245414.4:p.Trp11Arg
ENST00000437654.6:c.31T>A	ENSP00000405655.2:p.Trp11Arg
ENST00000613424.5:c.31T>A	ENSP00000480887.1:p.Trp11Arg
ENST00000638452.2:c.-169+39759A>T	ENSP00000492349.2:n.-169+39759A>T
ENST00000638504.1:n.206+69508A>T
ENST00000638568.2:c.-311+39759A>T	ENSP00000491158.2:n.-311+39759A>T
ENST00000639899.1:n.289+39759A>T
ENST00000640655.2:c.-169+2788A>T	ENSP00000491596.2:n.-169+2788A>T
ENST00000679440.1:c.31T>A	ENSP00000506401.1:p.Trp11Arg
ENST00000679499.1:c.31T>A	ENSP00000505066.1:p.Trp11Arg
ENST00000679921.1:c.-66+1097T>A	ENSP00000505766.1:n.-66+1097T>A
ENST00000680139.1:c.31T>A	ENSP00000506148.1:p.Trp11Arg
ENST00000680352.1:c.-7+1097T>A	ENSP00000506176.1:n.-7+1097T>A
ENST00000680796.1:c.31T>A	ENSP00000506572.1:p.Trp11Arg
ENST00000680903.1:c.31T>A	ENSP00000505720.1:p.Trp11Arg
ENST00000681584.1:c.31T>A	ENSP00000505448.1:p.Trp11Arg
ENST00000245414.8:c.31T>A	ENSP00000245414.4:p.Trp11Arg
ENST00000405885.6:c.31T>A	ENSP00000384406.1:p.Trp11Arg
ENST00000437654.5:c.31T>A	ENSP00000405655.1:p.Trp11Arg
ENST00000439555.2:c.31T>A	ENSP00000392455.1:p.Trp11Arg
ENST00000458069.5:c.31T>A	ENSP00000396318.1:p.Trp11Arg
ENST00000459982.5:n.257T>A
ENST00000463784.5:n.223+1097T>A
ENST00000476613.1:c.31T>A	ENSP00000473661.1:p.Trp11Arg
ENST00000493208.1:n.246T>A
ENST00000613424.4:c.31T>A	ENSP00000480887.1:p.Trp11Arg
NM_002198.2:c.31T>A	NP_002189.1:p.Trp11Arg
XM_011543378.1:c.31T>A	XP_011541680.1:p.Trp11Arg
XM_011543379.1:c.-66+1097T>A	XP_011541681.1:n.-66+1097T>A
XR_427711.2:n.265T>A
NM_001354924.1:c.31T>A	NP_001341853.1:p.Trp11Arg
NM_001354925.1:c.31T>A	NP_001341854.1:p.Trp11Arg
NR_149068.1:n.265T>A
NR_149069.1:n.265T>A
XM_011543379.2:c.-66+1097T>A	XP_011541681.1:n.-66+1097T>A
NM_002198.3:c.31T>A MANE Select	NP_002189.1:p.Trp11Arg
NR_149069.2:n.265T>A