Canonical Allele Identifier: CA2675209541

Gene: IRF1

Linked Data

• gnomAD v4: 5-132483643-C-CA

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132483644dup , CM000667.2:g.132483644dup	GRCh38
NC_000005.9:g.131819336dup , CM000667.1:g.131819336dup	GRCh37
NC_000005.8:g.131847235dup	NCBI36
NG_011450.1:g.12130dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000245414.9:c.*307dup MANE Select	ENSP00000245414.4:n.*307dup
ENST00000638452.2:c.-169+33955dup	ENSP00000492349.2:n.-169+33955dup
ENST00000638504.1:n.206+63704dup
ENST00000638568.2:c.-311+33955dup	ENSP00000491158.2:n.-311+33955dup
ENST00000639899.1:n.289+33955dup
ENST00000640655.2:c.-637-2548dup	ENSP00000491596.2:n.-637-2548dup
ENST00000679786.1:n.130+2913dup
ENST00000679921.1:c.292+2913dup	ENSP00000505766.1:n.292+2913dup
ENST00000679945.1:n.130+2913dup
ENST00000679964.1:n.50+2023dup
ENST00000680380.1:n.136+718dup
ENST00000680594.1:n.136+718dup
ENST00000681049.1:n.50+2023dup
ENST00000681634.1:n.136+718dup
ENST00000245414.8:c.*307dup	ENSP00000245414.4:n.*307dup
ENST00000405885.6:c.*307dup	ENSP00000384406.1:n.*307dup
ENST00000472045.1:n.4594dup
NM_002198.2:c.*307dup	NP_002189.1:n.*307dup
XM_011543378.1:c.*307dup	XP_011541680.1:n.*307dup
XM_011543379.1:c.*307dup	XP_011541681.1:n.*307dup
XR_427711.2:n.1346dup
NM_001354924.1:c.*307dup	NP_001341853.1:n.*307dup
NM_001354925.1:c.*307dup	NP_001341854.1:n.*307dup
NR_149068.1:n.1346dup
XM_011543379.2:c.*307dup	XP_011541681.1:n.*307dup
NM_002198.3:c.*307dup MANE Select	NP_002189.1:n.*307dup