Canonical Allele Identifier: CA565013984

Gene: IRF4

Linked Data

• dbSNP Id: rs1185988520
• gnomAD v2: 6-396567-GC-G
• gnomAD v3: 6-396567-GC-G
• gnomAD v4: 6-396567-GC-G
• MyVariant Identifiers: chr6:g.396568del (hg19) ; chr6:g.396568del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.396569del , CM000668.2:g.396569del	GRCh38
NC_000006.11:g.396569del , CM000668.1:g.396569del	GRCh37
NC_000006.10:g.341569del	NCBI36
NG_027728.1:g.9831del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000493114.2:c.493-542del	ENSP00000436094.2:n.493-542del
ENST00000696871.1:c.493-542del	ENSP00000512940.1:n.493-542del
ENST00000696872.1:c.553-539del	ENSP00000512941.1:n.553-539del
ENST00000696873.1:c.58-539del	ENSP00000512942.1:n.58-539del
ENST00000380956.9:c.493-539del MANE Select	ENSP00000370343.4:n.493-539del
ENST00000380956.8:c.493-539del	ENSP00000370343.4:n.493-539del
ENST00000493114.1:c.493-539del	ENSP00000436094.1:n.493-539del
ENST00000495137.5:n.319-539del
NM_001195286.1:c.493-542del	NP_001182215.1:n.493-542del
NM_002460.3:c.493-539del	NP_002451.2:n.493-539del
NR_046000.2:n.619-542del
XM_006715090.1:c.493-539del	XP_006715153.1:n.493-539del
XM_006715090.2:c.493-539del	XP_006715153.1:n.493-539del
NM_002460.4:c.493-539del MANE Select	NP_002451.2:n.493-539del
NM_001195286.2:c.493-542del	NP_001182215.1:n.493-542del
NR_046000.3:n.606-542del