Canonical Allele Identifier: CA1742565567

Gene: IRF5

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.128949424C= , CM000669.2:g.128949424C=	GRCh38
NC_000007.13:g.128589478C= , CM000669.1:g.128589478C=	GRCh37
NC_000007.12:g.128376714C=	NCBI36
NG_012306.1:g.16485C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700148.1:n.2387C=
ENST00000700151.1:n.4653C=
ENST00000700152.1:n.4193C=
ENST00000700153.1:n.3567C=
ENST00000700154.1:n.1731C=
ENST00000357234.10:c.*606C= MANE Select	ENSP00000349770.5:n.*606C=
ENST00000489702.6:c.*606C=	ENSP00000418037.2:n.*606C=
ENST00000249375.8:c.*606C=	ENSP00000249375.4:n.*606C=
ENST00000402030.6:c.*606C=	ENSP00000385352.2:n.*606C=
NM_001098627.3:c.*606C=	NP_001092097.2:n.*606C=
NM_001098629.2:c.*606C=	NP_001092099.1:n.*606C=
NM_001098630.2:c.*606C=	NP_001092100.1:n.*606C=
NM_001242452.2:c.*606C=	NP_001229381.1:n.*606C=
NM_032643.4:c.*606C=	NP_116032.1:n.*606C=
XM_005250317.2:c.*606C=	XP_005250374.1:n.*606C=
XM_006715974.2:c.*606C=	XP_006716037.1:n.*606C=
XM_011516158.1:c.*606C=	XP_011514460.1:n.*606C=
XM_011516159.1:c.*606C=	XP_011514461.1:n.*606C=
XM_011516160.1:c.*606C=	XP_011514462.1:n.*606C=
XM_011516161.1:c.*606C=	XP_011514463.1:n.*606C=
XM_011516162.1:c.*606C=	XP_011514464.1:n.*606C=
XM_011516163.1:c.*606C=	XP_011514465.1:n.*606C=
XM_011516164.1:c.*606C=	XP_011514466.1:n.*606C=
NM_001347928.1:c.*606C=	NP_001334857.1:n.*606C=
NM_001364314.1:c.*606C=	NP_001351243.1:n.*606C=
XM_011516158.3:c.*606C=	XP_011514460.1:n.*606C=
XM_011516159.3:c.*606C=	XP_011514461.1:n.*606C=
NM_001098629.3:c.*606C= MANE Select	NP_001092099.1:n.*606C=
NM_001098630.3:c.*606C=	NP_001092100.1:n.*606C=
NM_001242452.3:c.*606C=	NP_001229381.1:n.*606C=
NM_001347928.2:c.*606C=	NP_001334857.1:n.*606C=
NM_001364314.2:c.*606C=	NP_001351243.1:n.*606C=
NM_001098627.4:c.*606C=	NP_001092097.2:n.*606C=
NM_032643.5:c.*606C=	NP_116032.1:n.*606C=