Canonical Allele Identifier: CA1605235674
Gene: IRF4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.396296A= , CM000668.2:g.396296A= GRCh38
NC_000006.11:g.396296A= , CM000668.1:g.396296A= GRCh37
NC_000006.10:g.341296A= NCBI36
NG_027728.1:g.9558A=

Transcript Alleles

HGVS Amino-acid change
ENST00000493114.2:c.492+361A= ENSP00000436094.2:n.492+361A=
ENST00000696871.1:c.492+361A= ENSP00000512940.1:n.492+361A=
ENST00000696872.1:c.552+361A= ENSP00000512941.1:n.552+361A=
ENST00000696873.1:c.57+361A= ENSP00000512942.1:n.57+361A=
ENST00000380956.9:c.492+361A= MANE Select ENSP00000370343.4:n.492+361A=
ENST00000380956.8:c.492+361A= ENSP00000370343.4:n.492+361A=
ENST00000493114.1:c.492+361A= ENSP00000436094.1:n.492+361A=
ENST00000495137.5:n.318+361A=
NM_001195286.1:c.492+361A= NP_001182215.1:n.492+361A=
NM_002460.3:c.492+361A= NP_002451.2:n.492+361A=
NR_046000.2:n.618+361A=
XM_006715090.1:c.492+361A= XP_006715153.1:n.492+361A=
XM_006715090.2:c.492+361A= XP_006715153.1:n.492+361A=
NM_002460.4:c.492+361A= MANE Select NP_002451.2:n.492+361A=
NM_001195286.2:c.492+361A= NP_001182215.1:n.492+361A=
NR_046000.3:n.605+361A=