Canonical Allele Identifier: CA2675209702

Gene: IRF1

Linked Data

• gnomAD v4: 5-132483760-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132483760G>T , CM000667.2:g.132483760G>T	GRCh38
NC_000005.9:g.131819452G>T , CM000667.1:g.131819452G>T	GRCh37
NC_000005.8:g.131847351G>T	NCBI36
NG_011450.1:g.12014C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000245414.9:c.*191C>A MANE Select	ENSP00000245414.4:n.*191C>A
ENST00000638452.2:c.-169+34071G>T	ENSP00000492349.2:n.-169+34071G>T
ENST00000638504.1:n.206+63820G>T
ENST00000638568.2:c.-311+34071G>T	ENSP00000491158.2:n.-311+34071G>T
ENST00000639899.1:n.289+34071G>T
ENST00000640655.2:c.-637-2432G>T	ENSP00000491596.2:n.-637-2432G>T
ENST00000679786.1:n.130+2797C>A
ENST00000679921.1:c.292+2797C>A	ENSP00000505766.1:n.292+2797C>A
ENST00000679945.1:n.130+2797C>A
ENST00000679964.1:n.50+1907C>A
ENST00000680380.1:n.136+602C>A
ENST00000680594.1:n.136+602C>A
ENST00000681049.1:n.50+1907C>A
ENST00000681634.1:n.136+602C>A
ENST00000245414.8:c.*191C>A	ENSP00000245414.4:n.*191C>A
ENST00000405885.6:c.*191C>A	ENSP00000384406.1:n.*191C>A
ENST00000472045.1:n.4478C>A
NM_002198.2:c.*191C>A	NP_002189.1:n.*191C>A
XM_011543378.1:c.*191C>A	XP_011541680.1:n.*191C>A
XM_011543379.1:c.*191C>A	XP_011541681.1:n.*191C>A
XR_427711.2:n.1230C>A
NM_001354924.1:c.*191C>A	NP_001341853.1:n.*191C>A
NM_001354925.1:c.*191C>A	NP_001341854.1:n.*191C>A
NR_149068.1:n.1230C>A
XM_011543379.2:c.*191C>A	XP_011541681.1:n.*191C>A
NM_002198.3:c.*191C>A MANE Select	NP_002189.1:n.*191C>A