Canonical Allele Identifier: CA2677040565

Gene: IRF4

Linked Data

• gnomAD v4: 6-396063-A-AAAACTT

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.396067_396068insTTAAAC , CM000668.2:g.396067_396068insTTAAAC	GRCh38
NC_000006.11:g.396067_396068insTTAAAC , CM000668.1:g.396067_396068insTTAAAC	GRCh37
NC_000006.10:g.341067_341068insTTAAAC	NCBI36
NG_027728.1:g.9329_9330insTTAAAC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000469834.2:n.712_713insTTAAAC
ENST00000493114.2:c.492+132_492+133insTTAAAC	ENSP00000436094.2:n.492+132_492+133insTTAAAC
ENST00000696871.1:c.492+132_492+133insTTAAAC	ENSP00000512940.1:n.492+132_492+133insTTAAAC
ENST00000696872.1:c.552+132_552+133insTTAAAC	ENSP00000512941.1:n.552+132_552+133insTTAAAC
ENST00000696873.1:c.57+132_57+133insTTAAAC	ENSP00000512942.1:n.57+132_57+133insTTAAAC
ENST00000380956.9:c.492+132_492+133insTTAAAC MANE Select	ENSP00000370343.4:n.492+132_492+133insTTAAAC
ENST00000380956.8:c.492+132_492+133insTTAAAC	ENSP00000370343.4:n.492+132_492+133insTTAAAC
ENST00000468485.5:n.466_467insTTAAAC
ENST00000493114.1:c.492+132_492+133insTTAAAC	ENSP00000436094.1:n.492+132_492+133insTTAAAC
ENST00000495137.5:n.318+132_318+133insTTAAAC
NM_001195286.1:c.492+132_492+133insTTAAAC	NP_001182215.1:n.492+132_492+133insTTAAAC
NM_002460.3:c.492+132_492+133insTTAAAC	NP_002451.2:n.492+132_492+133insTTAAAC
NR_046000.2:n.618+132_618+133insTTAAAC
XM_006715090.1:c.492+132_492+133insTTAAAC	XP_006715153.1:n.492+132_492+133insTTAAAC
XM_006715090.2:c.492+132_492+133insTTAAAC	XP_006715153.1:n.492+132_492+133insTTAAAC
NM_002460.4:c.492+132_492+133insTTAAAC MANE Select	NP_002451.2:n.492+132_492+133insTTAAAC
NM_001195286.2:c.492+132_492+133insTTAAAC	NP_001182215.1:n.492+132_492+133insTTAAAC
NR_046000.3:n.605+132_605+133insTTAAAC