Canonical Allele Identifier: CA2239533708

Gene: IRF8

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.85908569G= , CM000678.2:g.85908569G=	GRCh38
NC_000016.9:g.85942175G= , CM000678.1:g.85942175G=	GRCh37
NC_000016.8:g.84499676G=	NCBI36
NG_029333.1:g.14402G= , LRG_294:g.14402G=

Transcript Alleles

HGVS	Amino-acid Change
NM_002163.4:c.175-421G= MANE Select	NP_002154.1:n.175-421G=
ENST00000268638.10:c.175-421G= MANE Select	ENSP00000268638.4:n.175-421G=
NM_001363907.1:c.205-421G=	NP_001350836.1:n.205-421G=
NM_001363908.1:c.-332-421G=	NP_001350837.1:n.-332-421G=
NM_002163.2:c.175-421G= , LRG_294t1:c.175-421G=	NP_002154.1:n.175-421G=
NM_002163.3:c.175-421G=	NP_002154.1:n.175-421G=
ENST00000268638.9:c.175-421G=	ENSP00000268638.4:n.175-421G=
ENST00000563180.1:c.175-421G=	ENSP00000458047.1:n.175-421G=
ENST00000564056.1:n.60-421G=
ENST00000564617.5:c.175-421G=	ENSP00000455784.1:n.175-421G=
ENST00000564803.5:c.175-421G=	ENSP00000456992.1:n.175-421G=
ENST00000564803.6:c.175-421G=	ENSP00000456992.2:n.175-421G=
ENST00000566369.2:c.175-421G=	ENSP00000455048.2:n.175-421G=
ENST00000696884.1:c.175-421G=	ENSP00000512951.1:n.175-421G=
ENST00000696885.1:c.175-421G=	ENSP00000512952.1:n.175-421G=
ENST00000696886.1:n.225-421G=
ENST00000696887.1:c.175-421G=	ENSP00000512953.1:n.175-421G=
ENST00000696888.1:n.224-421G=
ENST00000696889.1:n.168-421G=