Canonical Allele Identifier: CA2618388258

Gene: IRAK4

Linked Data

• gnomAD v4: 12-43788913-T-G

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.43788913T>G , CM000674.2:g.43788913T>G	GRCh38
NC_000012.11:g.44182716T>G , CM000674.1:g.44182716T>G	GRCh37
NC_000012.10:g.42468983T>G	NCBI36
NG_009892.1:g.34970T>G , LRG_75:g.34970T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000696791.1:c.*3483T>G	ENSP00000512873.1:n.*3483T>G
ENST00000696792.1:c.2746T>G	ENSP00000512874.1:n.2746T>G
ENST00000696795.1:c.*1018+2356T>G	ENSP00000512876.1:n.*1018+2356T>G
ENST00000613694.5:c.*2198T>G MANE Select	ENSP00000479889.3:n.*2198T>G
ENST00000431837.5:c.*2198T>G	ENSP00000390327.1:n.*2198T>G
ENST00000613694.4:c.*2198T>G	ENSP00000479889.2:n.*2198T>G
NM_001114182.2:c.*2198T>G	NP_001107654.1:n.*2198T>G
NM_001145256.1:c.*2198T>G	NP_001138728.1:n.*2198T>G
NM_001145257.1:c.*2198T>G	NP_001138729.1:n.*2198T>G
NM_001145258.1:c.*2198T>G	NP_001138730.1:n.*2198T>G
NM_016123.3:c.*2198T>G , LRG_75t1:c.*2198T>G	NP_057207.2:n.*2198T>G
XM_005268943.3:c.*2198T>G	XP_005269000.1:n.*2198T>G
XM_005268944.3:c.*2198T>G	XP_005269001.1:n.*2198T>G
XM_005268945.3:c.*2198T>G	XP_005269002.1:n.*2198T>G
XM_005268946.3:c.*2198T>G	XP_005269003.1:n.*2198T>G
XM_005268947.3:c.*2198T>G	XP_005269004.1:n.*2198T>G
XM_005268948.2:c.*2198T>G	XP_005269005.1:n.*2198T>G
XM_005268949.2:c.*2198T>G	XP_005269006.1:n.*2198T>G
XM_006719438.2:c.*2198T>G	XP_006719501.1:n.*2198T>G
XM_006719439.2:c.*2198T>G	XP_006719502.1:n.*2198T>G
XM_011538431.1:c.*2198T>G	XP_011536733.1:n.*2198T>G
XM_011538432.1:c.*2198T>G	XP_011536734.1:n.*2198T>G
XM_011538433.1:c.*2198T>G	XP_011536735.1:n.*2198T>G
NM_001351338.1:c.*2198T>G	NP_001338267.1:n.*2198T>G
NM_001351339.1:c.*2198T>G	NP_001338268.1:n.*2198T>G
NM_001351340.1:c.*2198T>G	NP_001338269.1:n.*2198T>G
NM_001351341.1:c.*2198T>G	NP_001338270.1:n.*2198T>G
NM_001351342.1:c.*2198T>G	NP_001338271.1:n.*2198T>G
NM_001351343.1:c.*2198T>G	NP_001338272.1:n.*2198T>G
NM_001351344.1:c.*2198T>G	NP_001338273.1:n.*2198T>G
NM_001351345.1:c.*2198T>G	NP_001338274.1:n.*2198T>G
XM_005268944.4:c.*2198T>G	XP_005269001.1:n.*2198T>G
XM_005268945.4:c.*2198T>G	XP_005269002.1:n.*2198T>G
XM_006719438.3:c.*2198T>G	XP_006719501.1:n.*2198T>G
XM_006719440.2:c.*2198T>G	XP_006719503.1:n.*2198T>G
XM_006719442.2:c.*2198T>G	XP_006719505.1:n.*2198T>G
XM_011538431.2:c.*2198T>G	XP_011536733.1:n.*2198T>G
XM_011538433.2:c.*2198T>G	XP_011536735.1:n.*2198T>G
XM_017019390.2:c.*2198T>G	XP_016874879.1:n.*2198T>G
NM_016123.4:c.*2198T>G MANE Select	NP_057207.2:n.*2198T>G
NM_001114182.3:c.*2198T>G	NP_001107654.1:n.*2198T>G
NM_001145256.2:c.*2198T>G	NP_001138728.1:n.*2198T>G
NM_001145257.2:c.*2198T>G	NP_001138729.1:n.*2198T>G
NM_001145258.2:c.*2198T>G	NP_001138730.1:n.*2198T>G
NM_001351338.2:c.*2198T>G	NP_001338267.1:n.*2198T>G
NM_001351339.2:c.*2198T>G	NP_001338268.1:n.*2198T>G
NM_001351340.2:c.*2198T>G	NP_001338269.1:n.*2198T>G
NM_001351341.2:c.*2198T>G	NP_001338270.1:n.*2198T>G
NM_001351342.2:c.*2198T>G	NP_001338271.1:n.*2198T>G
NM_001351343.2:c.*2198T>G	NP_001338272.1:n.*2198T>G
NM_001351344.2:c.*2198T>G	NP_001338273.1:n.*2198T>G
NM_001351345.2:c.*2198T>G	NP_001338274.1:n.*2198T>G