Canonical Allele Identifier: CA1605235693

Gene: IRF4

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.396330_396331delinsCT , CM000668.2:g.396330_396331delinsCT	GRCh38
NC_000006.11:g.396330_396331delinsCT , CM000668.1:g.396330_396331delinsCT	GRCh37
NC_000006.10:g.341330_341331delinsCT	NCBI36
NG_027728.1:g.9592_9593delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000493114.2:c.492+395_492+396delinsCT	ENSP00000436094.2:n.492+395_492+396delinsCT
ENST00000696871.1:c.492+395_492+396delinsCT	ENSP00000512940.1:n.492+395_492+396delinsCT
ENST00000696872.1:c.552+395_552+396delinsCT	ENSP00000512941.1:n.552+395_552+396delinsCT
ENST00000696873.1:c.57+395_57+396delinsCT	ENSP00000512942.1:n.57+395_57+396delinsCT
ENST00000380956.9:c.492+395_492+396delinsCT MANE Select	ENSP00000370343.4:n.492+395_492+396delinsCT
ENST00000380956.8:c.492+395_492+396delinsCT	ENSP00000370343.4:n.492+395_492+396delinsCT
ENST00000493114.1:c.492+395_492+396delinsCT	ENSP00000436094.1:n.492+395_492+396delinsCT
ENST00000495137.5:n.318+395_318+396delinsCT
NM_001195286.1:c.492+395_492+396delinsCT	NP_001182215.1:n.492+395_492+396delinsCT
NM_002460.3:c.492+395_492+396delinsCT	NP_002451.2:n.492+395_492+396delinsCT
NR_046000.2:n.618+395_618+396delinsCT
XM_006715090.1:c.492+395_492+396delinsCT	XP_006715153.1:n.492+395_492+396delinsCT
XM_006715090.2:c.492+395_492+396delinsCT	XP_006715153.1:n.492+395_492+396delinsCT
NM_002460.4:c.492+395_492+396delinsCT MANE Select	NP_002451.2:n.492+395_492+396delinsCT
NM_001195286.2:c.492+395_492+396delinsCT	NP_001182215.1:n.492+395_492+396delinsCT
NR_046000.3:n.605+395_605+396delinsCT