Canonical Allele Identifier: CA1742596100

Gene: IRF5

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.128938164C= , CM000669.2:g.128938164C=	GRCh38
NC_000007.13:g.128578218C= , CM000669.1:g.128578218C=	GRCh37
NC_000007.12:g.128365454C=	NCBI36
NG_012306.1:g.5225C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000700148.1:n.52+330C=
ENST00000357234.10:c.-12+115C= MANE Select	ENSP00000349770.5:n.-12+115C=
ENST00000489702.6:c.-12+330C=	ENSP00000418037.2:n.-12+330C=
ENST00000652142.1:n.21+115C=
ENST00000652525.1:c.-12+470C=	ENSP00000498293.1:n.-12+470C=
ENST00000357234.9:c.-12+115C=	ENSP00000349770.5:n.-12+115C=
ENST00000402030.6:c.-12+115C=	ENSP00000385352.2:n.-12+115C=
ENST00000461416.1:n.69+115C=
ENST00000464557.5:c.-158+115C=	ENSP00000419056.1:n.-158+115C=
ENST00000473787.5:c.-12+115C=	ENSP00000420274.1:n.-12+115C=
ENST00000477535.5:c.-12+115C=	ENSP00000419950.1:n.-12+115C=
ENST00000479582.5:c.-125+115C=	ENSP00000417770.1:n.-125+115C=
ENST00000488569.5:n.113+115C=
ENST00000489702.5:c.-12+330C=	ENSP00000418037.1:n.-12+330C=
ENST00000613821.4:c.-12+115C=	ENSP00000480058.1:n.-12+115C=
NM_001098629.2:c.-12+115C=	NP_001092099.1:n.-12+115C=
NM_001098630.2:c.-12+115C=	NP_001092100.1:n.-12+115C=
NM_001242452.2:c.-12+115C=	NP_001229381.1:n.-12+115C=
XM_006715974.2:c.-93C=	XP_006716037.1:n.-93C=
XM_011516160.1:c.-12+330C=	XP_011514462.1:n.-12+330C=
XM_011516161.1:c.-12+115C=	XP_011514463.1:n.-12+115C=
XM_011516162.1:c.-12+115C=	XP_011514464.1:n.-12+115C=
XM_011516164.1:c.-93C=	XP_011514466.1:n.-93C=
NM_001347928.1:c.-12+899C=	NP_001334857.1:n.-12+899C=
NM_001098629.3:c.-12+115C= MANE Select	NP_001092099.1:n.-12+115C=
NM_001098630.3:c.-12+115C=	NP_001092100.1:n.-12+115C=
NM_001242452.3:c.-12+115C=	NP_001229381.1:n.-12+115C=
NM_001347928.2:c.-12+899C=	NP_001334857.1:n.-12+899C=