Canonical Allele Identifier: CA1605235573

Gene: IRF4

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.396056G= , CM000668.2:g.396056G=	GRCh38
NC_000006.11:g.396056G= , CM000668.1:g.396056G=	GRCh37
NC_000006.10:g.341056G=	NCBI36
NG_027728.1:g.9318G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000469834.2:n.701G=
ENST00000493114.2:c.492+121G=	ENSP00000436094.2:n.492+121G=
ENST00000696871.1:c.492+121G=	ENSP00000512940.1:n.492+121G=
ENST00000696872.1:c.552+121G=	ENSP00000512941.1:n.552+121G=
ENST00000696873.1:c.57+121G=	ENSP00000512942.1:n.57+121G=
ENST00000380956.9:c.492+121G= MANE Select	ENSP00000370343.4:n.492+121G=
ENST00000380956.8:c.492+121G=	ENSP00000370343.4:n.492+121G=
ENST00000468485.5:n.455G=
ENST00000493114.1:c.492+121G=	ENSP00000436094.1:n.492+121G=
ENST00000495137.5:n.318+121G=
NM_001195286.1:c.492+121G=	NP_001182215.1:n.492+121G=
NM_002460.3:c.492+121G=	NP_002451.2:n.492+121G=
NR_046000.2:n.618+121G=
XM_006715090.1:c.492+121G=	XP_006715153.1:n.492+121G=
XM_006715090.2:c.492+121G=	XP_006715153.1:n.492+121G=
NM_002460.4:c.492+121G= MANE Select	NP_002451.2:n.492+121G=
NM_001195286.2:c.492+121G=	NP_001182215.1:n.492+121G=
NR_046000.3:n.605+121G=