Canonical Allele Identifier: CA2239530790

Gene: IRF8

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.85903024C= , CM000678.2:g.85903024C=	GRCh38
NC_000016.9:g.85936630C= , CM000678.1:g.85936630C=	GRCh37
NC_000016.8:g.84494131C=	NCBI36
NG_029333.1:g.8857C= , LRG_294:g.8857C=

Transcript Alleles

HGVS	Amino-acid Change
NM_002163.4:c.9C= MANE Select	NP_002154.1:p.Asp3=
ENST00000268638.10:c.9C= MANE Select	ENSP00000268638.4:p.Asp3=
NM_001363907.1:c.39C=	NP_001350836.1:p.Asp13=
NM_001363908.1:c.-498C=	NP_001350837.1:n.-498C=
NM_002163.2:c.9C= , LRG_294t1:c.9C=	NP_002154.1:p.Asp3=
NM_002163.3:c.9C=	NP_002154.1:p.Asp3=
ENST00000268638.9:c.9C=	ENSP00000268638.4:p.Asp3=
ENST00000563180.1:c.9C=	ENSP00000458047.1:p.Asp3=
ENST00000564617.5:c.9C=	ENSP00000455784.1:p.Asp3=
ENST00000564803.5:c.9C=	ENSP00000456992.1:p.Asp3=
ENST00000564803.6:c.9C=	ENSP00000456992.2:p.Asp3=
ENST00000565552.1:c.9C=	ENSP00000455816.1:p.Asp3=
ENST00000566369.2:c.9C=	ENSP00000455048.2:p.Asp3=
ENST00000570088.1:n.46C=
ENST00000696884.1:c.9C=	ENSP00000512951.1:p.Asp3=
ENST00000696885.1:c.9C=	ENSP00000512952.1:p.Asp3=
ENST00000696886.1:n.59C=
ENST00000696887.1:c.9C=	ENSP00000512953.1:p.Asp3=
ENST00000696888.1:n.58C=
ENST00000696889.1:n.2C=