Canonical Allele Identifier: CA1605235669
Gene: IRF4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.396287C= , CM000668.2:g.396287C= GRCh38
NC_000006.11:g.396287C= , CM000668.1:g.396287C= GRCh37
NC_000006.10:g.341287C= NCBI36
NG_027728.1:g.9549C=

Transcript Alleles

HGVS Amino-acid change
ENST00000493114.2:c.492+352C= ENSP00000436094.2:n.492+352C=
ENST00000696871.1:c.492+352C= ENSP00000512940.1:n.492+352C=
ENST00000696872.1:c.552+352C= ENSP00000512941.1:n.552+352C=
ENST00000696873.1:c.57+352C= ENSP00000512942.1:n.57+352C=
ENST00000380956.9:c.492+352C= MANE Select ENSP00000370343.4:n.492+352C=
ENST00000380956.8:c.492+352C= ENSP00000370343.4:n.492+352C=
ENST00000493114.1:c.492+352C= ENSP00000436094.1:n.492+352C=
ENST00000495137.5:n.318+352C=
NM_001195286.1:c.492+352C= NP_001182215.1:n.492+352C=
NM_002460.3:c.492+352C= NP_002451.2:n.492+352C=
NR_046000.2:n.618+352C=
XM_006715090.1:c.492+352C= XP_006715153.1:n.492+352C=
XM_006715090.2:c.492+352C= XP_006715153.1:n.492+352C=
NM_002460.4:c.492+352C= MANE Select NP_002451.2:n.492+352C=
NM_001195286.2:c.492+352C= NP_001182215.1:n.492+352C=
NR_046000.3:n.605+352C=