Canonical Allele Identifier: CA2578476157

Gene: IRF1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132483865del , CM000667.2:g.132483865del	GRCh38
NC_000005.9:g.131819557del , CM000667.1:g.131819557del	GRCh37
NC_000005.8:g.131847456del	NCBI36
NG_011450.1:g.11911del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000245414.9:c.*88del MANE Select	ENSP00000245414.4:n.*88del
ENST00000638452.2:c.-169+34176del	ENSP00000492349.2:n.-169+34176del
ENST00000638504.1:n.206+63925del
ENST00000638568.2:c.-311+34176del	ENSP00000491158.2:n.-311+34176del
ENST00000639899.1:n.289+34176del
ENST00000640655.2:c.-637-2327del	ENSP00000491596.2:n.-637-2327del
ENST00000679786.1:n.130+2694del
ENST00000679921.1:c.292+2694del	ENSP00000505766.1:n.292+2694del
ENST00000679945.1:n.130+2694del
ENST00000679964.1:n.50+1804del
ENST00000680139.1:c.*88del	ENSP00000506148.1:n.*88del
ENST00000680380.1:n.136+499del
ENST00000680562.1:c.514del	ENSP00000505853.1:n.514del
ENST00000680594.1:n.136+499del
ENST00000680903.1:c.*88del	ENSP00000505720.1:n.*88del
ENST00000681049.1:n.50+1804del
ENST00000681240.1:c.316del	ENSP00000506034.1:n.316del
ENST00000681336.1:c.313del	ENSP00000505242.1:n.313del
ENST00000681634.1:n.136+499del
ENST00000681694.1:c.378del	ENSP00000506552.1:n.378del
ENST00000245414.8:c.*88del	ENSP00000245414.4:n.*88del
ENST00000405885.6:c.*88del	ENSP00000384406.1:n.*88del
ENST00000472045.1:n.4375del
NM_002198.2:c.*88del	NP_002189.1:n.*88del
XM_011543378.1:c.*88del	XP_011541680.1:n.*88del
XM_011543379.1:c.*88del	XP_011541681.1:n.*88del
XR_427711.2:n.1127del
NM_001354924.1:c.*88del	NP_001341853.1:n.*88del
NM_001354925.1:c.*88del	NP_001341854.1:n.*88del
NR_149068.1:n.1127del
XM_011543379.2:c.*88del	XP_011541681.1:n.*88del
NM_002198.3:c.*88del MANE Select	NP_002189.1:n.*88del