Canonical Allele Identifier: CA1605235572

Gene: IRF4

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.396053A= , CM000668.2:g.396053A=	GRCh38
NC_000006.11:g.396053A= , CM000668.1:g.396053A=	GRCh37
NC_000006.10:g.341053A=	NCBI36
NG_027728.1:g.9315A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000469834.2:n.698A=
ENST00000493114.2:c.492+118A=	ENSP00000436094.2:n.492+118A=
ENST00000696871.1:c.492+118A=	ENSP00000512940.1:n.492+118A=
ENST00000696872.1:c.552+118A=	ENSP00000512941.1:n.552+118A=
ENST00000696873.1:c.57+118A=	ENSP00000512942.1:n.57+118A=
ENST00000380956.9:c.492+118A= MANE Select	ENSP00000370343.4:n.492+118A=
ENST00000380956.8:c.492+118A=	ENSP00000370343.4:n.492+118A=
ENST00000468485.5:n.452A=
ENST00000493114.1:c.492+118A=	ENSP00000436094.1:n.492+118A=
ENST00000495137.5:n.318+118A=
NM_001195286.1:c.492+118A=	NP_001182215.1:n.492+118A=
NM_002460.3:c.492+118A=	NP_002451.2:n.492+118A=
NR_046000.2:n.618+118A=
XM_006715090.1:c.492+118A=	XP_006715153.1:n.492+118A=
XM_006715090.2:c.492+118A=	XP_006715153.1:n.492+118A=
NM_002460.4:c.492+118A= MANE Select	NP_002451.2:n.492+118A=
NM_001195286.2:c.492+118A=	NP_001182215.1:n.492+118A=
NR_046000.3:n.605+118A=