Canonical Allele Identifier: CA2579831173

Gene: IRF4

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.396526T>C , CM000668.2:g.396526T>C	GRCh38
NC_000006.11:g.396526T>C , CM000668.1:g.396526T>C	GRCh37
NC_000006.10:g.341526T>C	NCBI36
NG_027728.1:g.9788T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000493114.2:c.493-585T>C	ENSP00000436094.2:n.493-585T>C
ENST00000696871.1:c.493-585T>C	ENSP00000512940.1:n.493-585T>C
ENST00000696872.1:c.553-582T>C	ENSP00000512941.1:n.553-582T>C
ENST00000696873.1:c.58-582T>C	ENSP00000512942.1:n.58-582T>C
ENST00000380956.9:c.493-582T>C MANE Select	ENSP00000370343.4:n.493-582T>C
ENST00000380956.8:c.493-582T>C	ENSP00000370343.4:n.493-582T>C
ENST00000493114.1:c.493-582T>C	ENSP00000436094.1:n.493-582T>C
ENST00000495137.5:n.319-582T>C
NM_001195286.1:c.493-585T>C	NP_001182215.1:n.493-585T>C
NM_002460.3:c.493-582T>C	NP_002451.2:n.493-582T>C
NR_046000.2:n.619-585T>C
XM_006715090.1:c.493-582T>C	XP_006715153.1:n.493-582T>C
XM_006715090.2:c.493-582T>C	XP_006715153.1:n.493-582T>C
NM_002460.4:c.493-582T>C MANE Select	NP_002451.2:n.493-582T>C
NM_001195286.2:c.493-585T>C	NP_001182215.1:n.493-585T>C
NR_046000.3:n.606-585T>C