Canonical Allele Identifier: CA1605235571

Gene: IRF4

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.396051C= , CM000668.2:g.396051C=	GRCh38
NC_000006.11:g.396051C= , CM000668.1:g.396051C=	GRCh37
NC_000006.10:g.341051C=	NCBI36
NG_027728.1:g.9313C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000469834.2:n.696C=
ENST00000493114.2:c.492+116C=	ENSP00000436094.2:n.492+116C=
ENST00000696871.1:c.492+116C=	ENSP00000512940.1:n.492+116C=
ENST00000696872.1:c.552+116C=	ENSP00000512941.1:n.552+116C=
ENST00000696873.1:c.57+116C=	ENSP00000512942.1:n.57+116C=
ENST00000380956.9:c.492+116C= MANE Select	ENSP00000370343.4:n.492+116C=
ENST00000380956.8:c.492+116C=	ENSP00000370343.4:n.492+116C=
ENST00000468485.5:n.450C=
ENST00000493114.1:c.492+116C=	ENSP00000436094.1:n.492+116C=
ENST00000495137.5:n.318+116C=
NM_001195286.1:c.492+116C=	NP_001182215.1:n.492+116C=
NM_002460.3:c.492+116C=	NP_002451.2:n.492+116C=
NR_046000.2:n.618+116C=
XM_006715090.1:c.492+116C=	XP_006715153.1:n.492+116C=
XM_006715090.2:c.492+116C=	XP_006715153.1:n.492+116C=
NM_002460.4:c.492+116C= MANE Select	NP_002451.2:n.492+116C=
NM_001195286.2:c.492+116C=	NP_001182215.1:n.492+116C=
NR_046000.3:n.605+116C=