Canonical Allele Identifier: CA824571507
Gene: IRF4 HGNC NCBI

Linked Data

dbSNP Id: rs1289733946
gnomAD v3: 6-396224-T-TA
gnomAD v4: 6-396224-T-TA

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.396224_396225insA , CM000668.2:g.396224_396225insA GRCh38
NC_000006.11:g.396224_396225insA , CM000668.1:g.396224_396225insA GRCh37
NC_000006.10:g.341224_341225insA NCBI36
NG_027728.1:g.9486_9487insA

Transcript Alleles

HGVS Amino-acid change
ENST00000493114.2:c.492+289_492+290insA ENSP00000436094.2:n.492+289_492+290insA
ENST00000696871.1:c.492+289_492+290insA ENSP00000512940.1:n.492+289_492+290insA
ENST00000696872.1:c.552+289_552+290insA ENSP00000512941.1:n.552+289_552+290insA
ENST00000696873.1:c.57+289_57+290insA ENSP00000512942.1:n.57+289_57+290insA
ENST00000380956.9:c.492+289_492+290insA MANE Select ENSP00000370343.4:n.492+289_492+290insA
ENST00000380956.8:c.492+289_492+290insA ENSP00000370343.4:n.492+289_492+290insA
ENST00000493114.1:c.492+289_492+290insA ENSP00000436094.1:n.492+289_492+290insA
ENST00000495137.5:n.318+289_318+290insA
NM_001195286.1:c.492+289_492+290insA NP_001182215.1:n.492+289_492+290insA
NM_002460.3:c.492+289_492+290insA NP_002451.2:n.492+289_492+290insA
NR_046000.2:n.618+289_618+290insA
XM_006715090.1:c.492+289_492+290insA XP_006715153.1:n.492+289_492+290insA
XM_006715090.2:c.492+289_492+290insA XP_006715153.1:n.492+289_492+290insA
NM_002460.4:c.492+289_492+290insA MANE Select NP_002451.2:n.492+289_492+290insA
NM_001195286.2:c.492+289_492+290insA NP_001182215.1:n.492+289_492+290insA
NR_046000.3:n.605+289_605+290insA