Canonical Allele Identifier: CA1605234181

Gene: IRF4

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.393388G>T , CM000668.2:g.393388G>T	GRCh38
NC_000006.11:g.393388G>T , CM000668.1:g.393388G>T	GRCh37
NC_000006.10:g.338388G>T	NCBI36
NG_027728.1:g.6650G>T

Transcript Alleles

HGVS	Amino-acid Change
NM_002460.4:c.216+20G>T MANE Select	NP_002451.2:n.216+20G>T
ENST00000380956.9:c.216+20G>T MANE Select	ENSP00000370343.4:n.216+20G>T
NM_001195286.1:c.216+20G>T	NP_001182215.1:n.216+20G>T
NM_001195286.2:c.216+20G>T	NP_001182215.1:n.216+20G>T
NM_002460.3:c.216+20G>T	NP_002451.2:n.216+20G>T
NR_046000.2:n.342+20G>T
NR_046000.3:n.329+20G>T
ENST00000380956.8:c.216+20G>T	ENSP00000370343.4:n.216+20G>T
ENST00000468485.5:n.59-1433G>T
ENST00000469834.1:n.90+20G>T
ENST00000469834.2:n.304+20G>T
ENST00000493114.1:c.216+20G>T	ENSP00000436094.1:n.216+20G>T
ENST00000493114.2:c.216+20G>T	ENSP00000436094.2:n.216+20G>T
ENST00000495137.5:n.43-1433G>T
ENST00000696871.1:c.216+20G>T	ENSP00000512940.1:n.216+20G>T
ENST00000696872.1:c.216+20G>T	ENSP00000512941.1:n.216+20G>T
ENST00000696873.1:c.-219-1433G>T	ENSP00000512942.1:n.-219-1433G>T
XM_006715090.1:c.216+20G>T	XP_006715153.1:n.216+20G>T
XM_006715090.2:c.216+20G>T	XP_006715153.1:n.216+20G>T