Canonical Allele Identifier: CA2579831670
Gene: IRF4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.396279A= , CM000668.2:g.396279A= GRCh38
NC_000006.11:g.396279A= , CM000668.1:g.396279A= GRCh37
NC_000006.10:g.341279A= NCBI36
NG_027728.1:g.9541A=

Transcript Alleles

HGVS Amino-acid change
ENST00000493114.2:c.492+344A= ENSP00000436094.2:n.492+344A=
ENST00000696871.1:c.492+344A= ENSP00000512940.1:n.492+344A=
ENST00000696872.1:c.552+344A= ENSP00000512941.1:n.552+344A=
ENST00000696873.1:c.57+344A= ENSP00000512942.1:n.57+344A=
ENST00000380956.9:c.492+344A= MANE Select ENSP00000370343.4:n.492+344A=
ENST00000380956.8:c.492+344A= ENSP00000370343.4:n.492+344A=
ENST00000493114.1:c.492+344A= ENSP00000436094.1:n.492+344A=
ENST00000495137.5:n.318+344A=
NM_001195286.1:c.492+344A= NP_001182215.1:n.492+344A=
NM_002460.3:c.492+344A= NP_002451.2:n.492+344A=
NR_046000.2:n.618+344A=
XM_006715090.1:c.492+344A= XP_006715153.1:n.492+344A=
XM_006715090.2:c.492+344A= XP_006715153.1:n.492+344A=
NM_002460.4:c.492+344A= MANE Select NP_002451.2:n.492+344A=
NM_001195286.2:c.492+344A= NP_001182215.1:n.492+344A=
NR_046000.3:n.605+344A=