Canonical Allele Identifier: CA2677040560

Gene: IRF4

Linked Data

• gnomAD v4: 6-396057-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.396057C>A , CM000668.2:g.396057C>A	GRCh38
NC_000006.11:g.396057C>A , CM000668.1:g.396057C>A	GRCh37
NC_000006.10:g.341057C>A	NCBI36
NG_027728.1:g.9319C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000469834.2:n.702C>A
ENST00000493114.2:c.492+122C>A	ENSP00000436094.2:n.492+122C>A
ENST00000696871.1:c.492+122C>A	ENSP00000512940.1:n.492+122C>A
ENST00000696872.1:c.552+122C>A	ENSP00000512941.1:n.552+122C>A
ENST00000696873.1:c.57+122C>A	ENSP00000512942.1:n.57+122C>A
ENST00000380956.9:c.492+122C>A MANE Select	ENSP00000370343.4:n.492+122C>A
ENST00000380956.8:c.492+122C>A	ENSP00000370343.4:n.492+122C>A
ENST00000468485.5:n.456C>A
ENST00000493114.1:c.492+122C>A	ENSP00000436094.1:n.492+122C>A
ENST00000495137.5:n.318+122C>A
NM_001195286.1:c.492+122C>A	NP_001182215.1:n.492+122C>A
NM_002460.3:c.492+122C>A	NP_002451.2:n.492+122C>A
NR_046000.2:n.618+122C>A
XM_006715090.1:c.492+122C>A	XP_006715153.1:n.492+122C>A
XM_006715090.2:c.492+122C>A	XP_006715153.1:n.492+122C>A
NM_002460.4:c.492+122C>A MANE Select	NP_002451.2:n.492+122C>A
NM_001195286.2:c.492+122C>A	NP_001182215.1:n.492+122C>A
NR_046000.3:n.605+122C>A