Canonical Allele Identifier: CA133332383

Gene: IRF4

Linked Data

• dbSNP Id: rs1018821014
• MyVariant Identifiers: chr6:g.396533_396534insC (hg19) ; chr6:g.396533_396534insC (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.396539dup , CM000668.2:g.396539dup	GRCh38
NC_000006.11:g.396539dup , CM000668.1:g.396539dup	GRCh37
NC_000006.10:g.341539dup	NCBI36
NG_027728.1:g.9801dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000493114.2:c.493-572dup	ENSP00000436094.2:n.493-572dup
ENST00000696871.1:c.493-572dup	ENSP00000512940.1:n.493-572dup
ENST00000696872.1:c.553-569dup	ENSP00000512941.1:n.553-569dup
ENST00000696873.1:c.58-569dup	ENSP00000512942.1:n.58-569dup
ENST00000380956.9:c.493-569dup MANE Select	ENSP00000370343.4:n.493-569dup
ENST00000380956.8:c.493-569dup	ENSP00000370343.4:n.493-569dup
ENST00000493114.1:c.493-569dup	ENSP00000436094.1:n.493-569dup
ENST00000495137.5:n.319-569dup
NM_001195286.1:c.493-572dup	NP_001182215.1:n.493-572dup
NM_002460.3:c.493-569dup	NP_002451.2:n.493-569dup
NR_046000.2:n.619-572dup
XM_006715090.1:c.493-569dup	XP_006715153.1:n.493-569dup
XM_006715090.2:c.493-569dup	XP_006715153.1:n.493-569dup
NM_002460.4:c.493-569dup MANE Select	NP_002451.2:n.493-569dup
NM_001195286.2:c.493-572dup	NP_001182215.1:n.493-572dup
NR_046000.3:n.606-572dup