Canonical Allele Identifier: CA2777855710

Gene: IRF5

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.128948512_128948513insAG , CM000669.2:g.128948512_128948513insAG	GRCh38
NC_000007.13:g.128588566_128588567insAG , CM000669.1:g.128588566_128588567insAG	GRCh37
NC_000007.12:g.128375802_128375803insAG	NCBI36
NG_012306.1:g.15573_15574insAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700148.1:n.1536-61_1536-60insAG
ENST00000700151.1:n.3802-61_3802-60insAG
ENST00000700152.1:n.3342-61_3342-60insAG
ENST00000700153.1:n.2716-61_2716-60insAG
ENST00000700154.1:n.819_820insAG
ENST00000357234.10:c.1300-61_1300-60insAG MANE Select	ENSP00000349770.5:n.1300-61_1300-60insAG
ENST00000489702.6:c.1300-61_1300-60insAG	ENSP00000418037.2:n.1300-61_1300-60insAG
ENST00000249375.8:c.1252-61_1252-60insAG	ENSP00000249375.4:n.1252-61_1252-60insAG
ENST00000357234.9:c.1300-61_1300-60insAG	ENSP00000349770.5:n.1300-61_1300-60insAG
ENST00000402030.6:c.1252-61_1252-60insAG	ENSP00000385352.2:n.1252-61_1252-60insAG
ENST00000465603.5:c.*780-61_*780-60insAG	ENSP00000418534.1:n.*780-61_*780-60insAG
ENST00000473745.5:c.1252-61_1252-60insAG	ENSP00000419149.1:n.1252-61_1252-60insAG
ENST00000477535.5:c.994-61_994-60insAG	ENSP00000419950.1:n.994-61_994-60insAG
ENST00000619830.1:c.*750-61_*750-60insAG	ENSP00000483292.1:n.*750-61_*750-60insAG
NM_001098627.3:c.1252-61_1252-60insAG	NP_001092097.2:n.1252-61_1252-60insAG
NM_001098629.2:c.1300-61_1300-60insAG	NP_001092099.1:n.1300-61_1300-60insAG
NM_001098630.2:c.1252-61_1252-60insAG	NP_001092100.1:n.1252-61_1252-60insAG
NM_001242452.2:c.994-61_994-60insAG	NP_001229381.1:n.994-61_994-60insAG
NM_032643.4:c.1252-61_1252-60insAG	NP_116032.1:n.1252-61_1252-60insAG
XM_005250317.2:c.1300-61_1300-60insAG	XP_005250374.1:n.1300-61_1300-60insAG
XM_006715974.2:c.1300-61_1300-60insAG	XP_006716037.1:n.1300-61_1300-60insAG
XM_011516158.1:c.1300-61_1300-60insAG	XP_011514460.1:n.1300-61_1300-60insAG
XM_011516159.1:c.1300-61_1300-60insAG	XP_011514461.1:n.1300-61_1300-60insAG
XM_011516160.1:c.1300-61_1300-60insAG	XP_011514462.1:n.1300-61_1300-60insAG
XM_011516161.1:c.1270-61_1270-60insAG	XP_011514463.1:n.1270-61_1270-60insAG
XM_011516162.1:c.1222-61_1222-60insAG	XP_011514464.1:n.1222-61_1222-60insAG
XM_011516163.1:c.1222-61_1222-60insAG	XP_011514465.1:n.1222-61_1222-60insAG
XM_011516164.1:c.1222-61_1222-60insAG	XP_011514466.1:n.1222-61_1222-60insAG
NM_001347928.1:c.1300-61_1300-60insAG	NP_001334857.1:n.1300-61_1300-60insAG
NM_001364314.1:c.1300-61_1300-60insAG	NP_001351243.1:n.1300-61_1300-60insAG
XM_011516158.3:c.1300-61_1300-60insAG	XP_011514460.1:n.1300-61_1300-60insAG
XM_011516159.3:c.1300-61_1300-60insAG	XP_011514461.1:n.1300-61_1300-60insAG
NM_001098629.3:c.1300-61_1300-60insAG MANE Select	NP_001092099.1:n.1300-61_1300-60insAG
NM_001098630.3:c.1252-61_1252-60insAG	NP_001092100.1:n.1252-61_1252-60insAG
NM_001242452.3:c.994-61_994-60insAG	NP_001229381.1:n.994-61_994-60insAG
NM_001347928.2:c.1300-61_1300-60insAG	NP_001334857.1:n.1300-61_1300-60insAG
NM_001364314.2:c.1300-61_1300-60insAG	NP_001351243.1:n.1300-61_1300-60insAG
NM_001098627.4:c.1252-61_1252-60insAG	NP_001092097.2:n.1252-61_1252-60insAG
NM_032643.5:c.1252-61_1252-60insAG	NP_116032.1:n.1252-61_1252-60insAG