Canonical Allele Identifier: CA2684836845

Gene: IRF5

Linked Data

• gnomAD v4: 7-128938154-GGCCCCGC-G

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.128938160_128938166del , CM000669.2:g.128938160_128938166del	GRCh38
NC_000007.13:g.128578214_128578220del , CM000669.1:g.128578214_128578220del	GRCh37
NC_000007.12:g.128365450_128365456del	NCBI36
NG_012306.1:g.5221_5227del

Transcript Alleles

HGVS	Amino-acid change
ENST00000700148.1:n.52+326_52+332del
ENST00000357234.10:c.-12+111_-12+117del MANE Select	ENSP00000349770.5:n.-12+111_-12+117del
ENST00000489702.6:c.-12+326_-12+332del	ENSP00000418037.2:n.-12+326_-12+332del
ENST00000652142.1:n.21+111_21+117del
ENST00000652525.1:c.-12+466_-12+472del	ENSP00000498293.1:n.-12+466_-12+472del
ENST00000357234.9:c.-12+111_-12+117del	ENSP00000349770.5:n.-12+111_-12+117del
ENST00000402030.6:c.-12+111_-12+117del	ENSP00000385352.2:n.-12+111_-12+117del
ENST00000461416.1:n.69+111_69+117del
ENST00000464557.5:c.-158+111_-158+117del	ENSP00000419056.1:n.-158+111_-158+117del
ENST00000473787.5:c.-12+111_-12+117del	ENSP00000420274.1:n.-12+111_-12+117del
ENST00000477535.5:c.-12+111_-12+117del	ENSP00000419950.1:n.-12+111_-12+117del
ENST00000479582.5:c.-125+111_-125+117del	ENSP00000417770.1:n.-125+111_-125+117del
ENST00000488569.5:n.113+111_113+117del
ENST00000489702.5:c.-12+326_-12+332del	ENSP00000418037.1:n.-12+326_-12+332del
ENST00000613821.4:c.-12+111_-12+117del	ENSP00000480058.1:n.-12+111_-12+117del
NM_001098629.2:c.-12+111_-12+117del	NP_001092099.1:n.-12+111_-12+117del
NM_001098630.2:c.-12+111_-12+117del	NP_001092100.1:n.-12+111_-12+117del
NM_001242452.2:c.-12+111_-12+117del	NP_001229381.1:n.-12+111_-12+117del
XM_006715974.2:c.-97_-91del	XP_006716037.1:n.-97_-91del
XM_011516160.1:c.-12+326_-12+332del	XP_011514462.1:n.-12+326_-12+332del
XM_011516161.1:c.-12+111_-12+117del	XP_011514463.1:n.-12+111_-12+117del
XM_011516162.1:c.-12+111_-12+117del	XP_011514464.1:n.-12+111_-12+117del
XM_011516164.1:c.-97_-91del	XP_011514466.1:n.-97_-91del
NM_001347928.1:c.-12+895_-12+901del	NP_001334857.1:n.-12+895_-12+901del
NM_001098629.3:c.-12+111_-12+117del MANE Select	NP_001092099.1:n.-12+111_-12+117del
NM_001098630.3:c.-12+111_-12+117del	NP_001092100.1:n.-12+111_-12+117del
NM_001242452.3:c.-12+111_-12+117del	NP_001229381.1:n.-12+111_-12+117del
NM_001347928.2:c.-12+895_-12+901del	NP_001334857.1:n.-12+895_-12+901del