Canonical Allele Identifier: CA2579831311

Gene: IRF4

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.396570T>A , CM000668.2:g.396570T>A	GRCh38
NC_000006.11:g.396570T>A , CM000668.1:g.396570T>A	GRCh37
NC_000006.10:g.341570T>A	NCBI36
NG_027728.1:g.9832T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000493114.2:c.493-541T>A	ENSP00000436094.2:n.493-541T>A
ENST00000696871.1:c.493-541T>A	ENSP00000512940.1:n.493-541T>A
ENST00000696872.1:c.553-538T>A	ENSP00000512941.1:n.553-538T>A
ENST00000696873.1:c.58-538T>A	ENSP00000512942.1:n.58-538T>A
ENST00000380956.9:c.493-538T>A MANE Select	ENSP00000370343.4:n.493-538T>A
ENST00000380956.8:c.493-538T>A	ENSP00000370343.4:n.493-538T>A
ENST00000493114.1:c.493-538T>A	ENSP00000436094.1:n.493-538T>A
ENST00000495137.5:n.319-538T>A
NM_001195286.1:c.493-541T>A	NP_001182215.1:n.493-541T>A
NM_002460.3:c.493-538T>A	NP_002451.2:n.493-538T>A
NR_046000.2:n.619-541T>A
XM_006715090.1:c.493-538T>A	XP_006715153.1:n.493-538T>A
XM_006715090.2:c.493-538T>A	XP_006715153.1:n.493-538T>A
NM_002460.4:c.493-538T>A MANE Select	NP_002451.2:n.493-538T>A
NM_001195286.2:c.493-541T>A	NP_001182215.1:n.493-541T>A
NR_046000.3:n.606-541T>A