Canonical Allele Identifier: CA14255971

Gene: IRF8

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.85912844T>C , CM000678.2:g.85912844T>C	GRCh38
NC_000016.9:g.85946450T>C , CM000678.1:g.85946450T>C	GRCh37
NC_000016.8:g.84503951T>C	NCBI36
NG_029333.1:g.18677T>C , LRG_294:g.18677T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000564803.6:c.448-287T>C	ENSP00000456992.2:n.448-287T>C
ENST00000566369.2:c.447+1186T>C	ENSP00000455048.2:n.447+1186T>C
ENST00000696884.1:c.447+1186T>C	ENSP00000512951.1:n.447+1186T>C
ENST00000696885.1:c.*926-287T>C	ENSP00000512952.1:n.*926-287T>C
ENST00000696886.1:n.2581-287T>C
ENST00000696887.1:c.448-287T>C	ENSP00000512953.1:n.448-287T>C
ENST00000696888.1:n.840T>C
ENST00000696890.1:n.395-287T>C
ENST00000268638.10:c.448-287T>C MANE Select	ENSP00000268638.4:n.448-287T>C
ENST00000268638.9:c.448-287T>C	ENSP00000268638.4:n.448-287T>C
ENST00000564056.1:n.333-287T>C
ENST00000564617.5:c.448-287T>C	ENSP00000455784.1:n.448-287T>C
ENST00000564803.5:c.448-287T>C	ENSP00000456992.1:n.448-287T>C
ENST00000566369.1:c.275+1186T>C
NM_002163.2:c.448-287T>C , LRG_294t1:c.448-287T>C	NP_002154.1:n.448-287T>C
XM_011523064.1:c.-60+1186T>C	XP_011521366.1:n.-60+1186T>C
NM_001363907.1:c.478-287T>C	NP_001350836.1:n.478-287T>C
NM_001363908.1:c.-60+1186T>C	NP_001350837.1:n.-60+1186T>C
NM_002163.3:c.448-287T>C	NP_002154.1:n.448-287T>C
NM_002163.4:c.448-287T>C MANE Select	NP_002154.1:n.448-287T>C