Canonical Allele Identifier: CA2239533995

Gene: IRF8

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.85909137A= , CM000678.2:g.85909137A=	GRCh38
NC_000016.9:g.85942743A= , CM000678.1:g.85942743A=	GRCh37
NC_000016.8:g.84500244A=	NCBI36
NG_029333.1:g.14970A= , LRG_294:g.14970A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000564803.6:c.322A=	ENSP00000456992.2:p.Lys108=
ENST00000566369.2:c.322A=	ENSP00000455048.2:p.Lys108=
ENST00000696884.1:c.322A=	ENSP00000512951.1:p.Lys108=
ENST00000696885.1:c.322A=	ENSP00000512952.1:p.Lys108=
ENST00000696886.1:n.372A=
ENST00000696887.1:c.322A=	ENSP00000512953.1:p.Lys108=
ENST00000696888.1:n.371A=
ENST00000696889.1:n.315A=
ENST00000696890.1:n.269A=
ENST00000268638.10:c.322A= MANE Select	ENSP00000268638.4:p.Lys108=
ENST00000268638.9:c.322A=	ENSP00000268638.4:p.Lys108=
ENST00000563180.1:c.322A=	ENSP00000458047.1:p.Lys108=
ENST00000564056.1:n.207A=
ENST00000564617.5:c.322A=	ENSP00000455784.1:p.Lys108=
ENST00000564803.5:c.322A=	ENSP00000456992.1:p.Lys108=
ENST00000566369.1:c.150A=
NM_002163.2:c.322A= , LRG_294t1:c.322A=	NP_002154.1:p.Lys108=
NM_001363907.1:c.352A=	NP_001350836.1:p.Lys118=
NM_001363908.1:c.-185A=	NP_001350837.1:n.-185A=
NM_002163.3:c.322A=	NP_002154.1:p.Lys108=
NM_002163.4:c.322A= MANE Select	NP_002154.1:p.Lys108=