Canonical Allele Identifier: CA2677040537

Gene: IRF4

Linked Data

• gnomAD v4: 6-396035-T-TAGCAAATGGCAAG

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.396035_396036insAGCAAATGGCAAG , CM000668.2:g.396035_396036insAGCAAATGGCAAG	GRCh38
NC_000006.11:g.396035_396036insAGCAAATGGCAAG , CM000668.1:g.396035_396036insAGCAAATGGCAAG	GRCh37
NC_000006.10:g.341035_341036insAGCAAATGGCAAG	NCBI36
NG_027728.1:g.9297_9298insAGCAAATGGCAAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000469834.2:n.680_681insAGCAAATGGCAAG
ENST00000493114.2:c.492+100_492+101insAGCAAATGGCAAG	ENSP00000436094.2:n.492+100_492+101insAGCAAATGGCAAG
ENST00000696871.1:c.492+100_492+101insAGCAAATGGCAAG	ENSP00000512940.1:n.492+100_492+101insAGCAAATGGCAAG
ENST00000696872.1:c.552+100_552+101insAGCAAATGGCAAG	ENSP00000512941.1:n.552+100_552+101insAGCAAATGGCAAG
ENST00000696873.1:c.57+100_57+101insAGCAAATGGCAAG	ENSP00000512942.1:n.57+100_57+101insAGCAAATGGCAAG
ENST00000380956.9:c.492+100_492+101insAGCAAATGGCAAG MANE Select	ENSP00000370343.4:n.492+100_492+101insAGCAAATGGCAAG
ENST00000380956.8:c.492+100_492+101insAGCAAATGGCAAG	ENSP00000370343.4:n.492+100_492+101insAGCAAATGGCAAG
ENST00000468485.5:n.434_435insAGCAAATGGCAAG
ENST00000493114.1:c.492+100_492+101insAGCAAATGGCAAG	ENSP00000436094.1:n.492+100_492+101insAGCAAATGGCAAG
ENST00000495137.5:n.318+100_318+101insAGCAAATGGCAAG
NM_001195286.1:c.492+100_492+101insAGCAAATGGCAAG	NP_001182215.1:n.492+100_492+101insAGCAAATGGCAAG
NM_002460.3:c.492+100_492+101insAGCAAATGGCAAG	NP_002451.2:n.492+100_492+101insAGCAAATGGCAAG
NR_046000.2:n.618+100_618+101insAGCAAATGGCAAG
XM_006715090.1:c.492+100_492+101insAGCAAATGGCAAG	XP_006715153.1:n.492+100_492+101insAGCAAATGGCAAG
XM_006715090.2:c.492+100_492+101insAGCAAATGGCAAG	XP_006715153.1:n.492+100_492+101insAGCAAATGGCAAG
NM_002460.4:c.492+100_492+101insAGCAAATGGCAAG MANE Select	NP_002451.2:n.492+100_492+101insAGCAAATGGCAAG
NM_001195286.2:c.492+100_492+101insAGCAAATGGCAAG	NP_001182215.1:n.492+100_492+101insAGCAAATGGCAAG
NR_046000.3:n.605+100_605+101insAGCAAATGGCAAG