Canonical Allele Identifier: CA116178

Gene: IRF5

Linked Data

• PubMed: PMID:15657875 ; PMID:16642019 ; PMID:17599733 ; PMID:18063667

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.128938247T= , CM000669.2:g.128938247T=	GRCh38

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700148.1:n.52+413T=
ENST00000357234.10:c.-12+198T= MANE Select	ENSP00000349770.5:n.-12+198T=
ENST00000489702.6:c.-12+413T=	ENSP00000418037.2:n.-12+413T=
ENST00000650798.1:n.29+2T=
ENST00000652142.1:n.21+198T=
ENST00000652525.1:c.-12+553T=	ENSP00000498293.1:n.-12+553T=
ENST00000249375.8:c.-12+2T=	ENSP00000249375.4:n.-12+2T=
ENST00000357234.9:c.-12+198T=	ENSP00000349770.5:n.-12+198T=
ENST00000402030.6:c.-12+198T=	ENSP00000385352.2:n.-12+198T=
ENST00000461416.1:n.69+198T=
ENST00000464557.5:c.-158+198T=	ENSP00000419056.1:n.-158+198T=
ENST00000473787.5:c.-12+198T=	ENSP00000420274.1:n.-12+198T=
ENST00000477535.5:c.-12+198T=	ENSP00000419950.1:n.-12+198T=
ENST00000479582.5:c.-125+198T=	ENSP00000417770.1:n.-125+198T=
ENST00000488569.5:n.113+198T=
ENST00000489702.5:c.-12+413T=	ENSP00000418037.1:n.-12+413T=
ENST00000613821.4:c.-12+198T=	ENSP00000480058.1:n.-12+198T=
NM_001098629.2:c.-12+198T=	NP_001092099.1:n.-12+198T=
NM_001098630.2:c.-12+198T=	NP_001092100.1:n.-12+198T=
NM_001242452.2:c.-12+198T=	NP_001229381.1:n.-12+198T=
NM_032643.4:c.-12+2T=	NP_116032.1:n.-12+2T=
XM_006715974.2:c.-12+2T=	XP_006716037.1:n.-12+2T=
XM_011516160.1:c.-12+413T=	XP_011514462.1:n.-12+413T=
XM_011516161.1:c.-12+198T=	XP_011514463.1:n.-12+198T=
XM_011516162.1:c.-12+198T=	XP_011514464.1:n.-12+198T=
XM_011516164.1:c.-12+2T=	XP_011514466.1:n.-12+2T=
NM_001347928.1:c.-12+982T=	NP_001334857.1:n.-12+982T=
NM_001098629.3:c.-12+198T= MANE Select	NP_001092099.1:n.-12+198T=
NM_001098630.3:c.-12+198T=	NP_001092100.1:n.-12+198T=
NM_001242452.3:c.-12+198T=	NP_001229381.1:n.-12+198T=
NM_001347928.2:c.-12+982T=	NP_001334857.1:n.-12+982T=
NM_032643.5:c.-12+2T=	NP_116032.1:n.-12+2T=