Canonical Allele Identifier: CA833144292

Gene: IRF5

Linked Data

• dbSNP Id: rs1251709429
• MyVariant Identifiers: chr7:g.128589434_128589435del (hg19) ; chr7:g.128949380_128949381del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.128949383_128949384del , CM000669.2:g.128949383_128949384del	GRCh38
NC_000007.13:g.128589437_128589438del , CM000669.1:g.128589437_128589438del	GRCh37
NC_000007.12:g.128376673_128376674del	NCBI36
NG_012306.1:g.16444_16445del

Transcript Alleles

HGVS	Amino-acid change
ENST00000700148.1:n.2346_2347del
ENST00000700151.1:n.4612_4613del
ENST00000700152.1:n.4152_4153del
ENST00000700153.1:n.3526_3527del
ENST00000700154.1:n.1690_1691del
ENST00000357234.10:c.*565_*566del MANE Select	ENSP00000349770.5:n.*565_*566del
ENST00000489702.6:c.*565_*566del	ENSP00000418037.2:n.*565_*566del
ENST00000249375.8:c.*565_*566del	ENSP00000249375.4:n.*565_*566del
ENST00000402030.6:c.*565_*566del	ENSP00000385352.2:n.*565_*566del
ENST00000465603.5:c.*1590_*1591del	ENSP00000418534.1:n.*1590_*1591del
ENST00000473745.5:c.*565_*566del	ENSP00000419149.1:n.*565_*566del
NM_001098627.3:c.*565_*566del	NP_001092097.2:n.*565_*566del
NM_001098629.2:c.*565_*566del	NP_001092099.1:n.*565_*566del
NM_001098630.2:c.*565_*566del	NP_001092100.1:n.*565_*566del
NM_001242452.2:c.*565_*566del	NP_001229381.1:n.*565_*566del
NM_032643.4:c.*565_*566del	NP_116032.1:n.*565_*566del
XM_005250317.2:c.*565_*566del	XP_005250374.1:n.*565_*566del
XM_006715974.2:c.*565_*566del	XP_006716037.1:n.*565_*566del
XM_011516158.1:c.*565_*566del	XP_011514460.1:n.*565_*566del
XM_011516159.1:c.*565_*566del	XP_011514461.1:n.*565_*566del
XM_011516160.1:c.*565_*566del	XP_011514462.1:n.*565_*566del
XM_011516161.1:c.*565_*566del	XP_011514463.1:n.*565_*566del
XM_011516162.1:c.*565_*566del	XP_011514464.1:n.*565_*566del
XM_011516163.1:c.*565_*566del	XP_011514465.1:n.*565_*566del
XM_011516164.1:c.*565_*566del	XP_011514466.1:n.*565_*566del
NM_001347928.1:c.*565_*566del	NP_001334857.1:n.*565_*566del
NM_001364314.1:c.*565_*566del	NP_001351243.1:n.*565_*566del
XM_011516158.3:c.*565_*566del	XP_011514460.1:n.*565_*566del
XM_011516159.3:c.*565_*566del	XP_011514461.1:n.*565_*566del
NM_001098629.3:c.*565_*566del MANE Select	NP_001092099.1:n.*565_*566del
NM_001098630.3:c.*565_*566del	NP_001092100.1:n.*565_*566del
NM_001242452.3:c.*565_*566del	NP_001229381.1:n.*565_*566del
NM_001347928.2:c.*565_*566del	NP_001334857.1:n.*565_*566del
NM_001364314.2:c.*565_*566del	NP_001351243.1:n.*565_*566del
NM_001098627.4:c.*565_*566del	NP_001092097.2:n.*565_*566del
NM_032643.5:c.*565_*566del	NP_116032.1:n.*565_*566del