Canonical Allele Identifier: CA2032520658

Gene: IRAK4

Linked Data

• dbSNP Id: rs4251424

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.43760023C>G , CM000674.2:g.43760023C>G	GRCh38
NC_000012.11:g.44153826C>G , CM000674.1:g.44153826C>G	GRCh37
NC_000012.10:g.42440093C>G	NCBI36
NG_009892.1:g.6080C>G , LRG_75:g.6080C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696790.1:c.-57-902C>G	ENSP00000512872.1:n.-57-902C>G
ENST00000696791.1:c.-10+823C>G	ENSP00000512873.1:n.-10+823C>G
ENST00000613694.5:c.-10+1007C>G MANE Select	ENSP00000479889.3:n.-10+1007C>G
ENST00000431837.5:c.-236+1007C>G	ENSP00000390327.1:n.-236+1007C>G
ENST00000440781.6:c.-66+1007C>G	ENSP00000408734.2:n.-66+1007C>G
ENST00000546780.5:n.50+1007C>G
ENST00000547101.5:c.-10+1007C>G	ENSP00000449317.1:n.-10+1007C>G
ENST00000547521.5:c.-58+431C>G	ENSP00000449693.1:n.-58+431C>G
ENST00000550361.1:c.-10+823C>G	ENSP00000449859.1:n.-10+823C>G
ENST00000550386.5:c.-57-902C>G	ENSP00000449848.1:n.-57-902C>G
ENST00000550615.5:c.-10+1007C>G	ENSP00000449553.1:n.-10+1007C>G
ENST00000550616.5:c.-212-902C>G	ENSP00000446571.1:n.-212-902C>G
ENST00000551736.5:c.-57-902C>G	ENSP00000446490.1:n.-57-902C>G
ENST00000552309.5:c.-57-902C>G	ENSP00000448197.1:n.-57-902C>G
ENST00000613694.4:c.-10+1007C>G	ENSP00000479889.2:n.-10+1007C>G
NM_001114182.2:c.-57-902C>G	NP_001107654.1:n.-57-902C>G
NM_001145256.1:c.-283-902C>G	NP_001138728.1:n.-283-902C>G
NM_001145257.1:c.-236+1007C>G	NP_001138729.1:n.-236+1007C>G
NM_001145258.1:c.-66+1007C>G	NP_001138730.1:n.-66+1007C>G
NM_016123.3:c.-10+1007C>G , LRG_75t1:c.-10+1007C>G	NP_057207.2:n.-10+1007C>G
XM_005268943.3:c.-10+823C>G	XP_005269000.1:n.-10+823C>G
XM_005268944.3:c.-10+37C>G	XP_005269001.1:n.-10+37C>G
XM_005268945.3:c.-10+431C>G	XP_005269002.1:n.-10+431C>G
XM_005268947.3:c.-449+1007C>G	XP_005269004.1:n.-449+1007C>G
XM_005268948.2:c.-496-902C>G	XP_005269005.1:n.-496-902C>G
XM_005268949.2:c.-236+823C>G	XP_005269006.1:n.-236+823C>G
XM_006719438.2:c.-58+431C>G	XP_006719501.1:n.-58+431C>G
XM_006719439.2:c.-284+431C>G	XP_006719502.1:n.-284+431C>G
XM_006719440.1:c.-533+1007C>G	XP_006719503.1:n.-533+1007C>G
XM_006719441.1:c.-387+1007C>G	XP_006719504.1:n.-387+1007C>G
XM_006719442.1:c.-434-902C>G	XP_006719505.1:n.-434-902C>G
XM_006719443.2:c.-387+823C>G	XP_006719506.1:n.-387+823C>G
XM_011538431.1:c.-58+37C>G	XP_011536733.1:n.-58+37C>G
XM_011538432.1:c.-58+823C>G	XP_011536734.1:n.-58+823C>G
NM_001351338.1:c.-284+431C>G	NP_001338267.1:n.-284+431C>G
NM_001351339.1:c.-496-902C>G	NP_001338268.1:n.-496-902C>G
NM_001351340.1:c.-449+1007C>G	NP_001338269.1:n.-449+1007C>G
NM_001351341.1:c.-449+823C>G	NP_001338270.1:n.-449+823C>G
NM_001351342.1:c.-279+1007C>G	NP_001338271.1:n.-279+1007C>G
NM_001351343.1:c.-387+823C>G	NP_001338272.1:n.-387+823C>G
NM_001351344.1:c.-387+1007C>G	NP_001338273.1:n.-387+1007C>G
NM_001351345.1:c.-58+823C>G	NP_001338274.1:n.-58+823C>G
XM_005268944.4:c.-10+37C>G	XP_005269001.1:n.-10+37C>G
XM_005268945.4:c.-10+431C>G	XP_005269002.1:n.-10+431C>G
XM_006719438.3:c.-58+431C>G	XP_006719501.1:n.-58+431C>G
XM_006719440.2:c.-533+1007C>G	XP_006719503.1:n.-533+1007C>G
XM_006719442.2:c.-434-902C>G	XP_006719505.1:n.-434-902C>G
XM_011538431.2:c.-58+37C>G	XP_011536733.1:n.-58+37C>G
XM_017019390.2:c.-212-902C>G	XP_016874879.1:n.-212-902C>G
XM_024449008.1:c.-57-902C>G	XP_024304776.1:n.-57-902C>G
NM_016123.4:c.-10+1007C>G MANE Select	NP_057207.2:n.-10+1007C>G
NM_001114182.3:c.-57-902C>G	NP_001107654.1:n.-57-902C>G
NM_001145256.2:c.-283-902C>G	NP_001138728.1:n.-283-902C>G
NM_001145257.2:c.-236+1007C>G	NP_001138729.1:n.-236+1007C>G
NM_001145258.2:c.-66+1007C>G	NP_001138730.1:n.-66+1007C>G
NM_001351338.2:c.-284+431C>G	NP_001338267.1:n.-284+431C>G
NM_001351339.2:c.-496-902C>G	NP_001338268.1:n.-496-902C>G
NM_001351340.2:c.-449+1007C>G	NP_001338269.1:n.-449+1007C>G
NM_001351341.2:c.-449+823C>G	NP_001338270.1:n.-449+823C>G
NM_001351342.2:c.-279+1007C>G	NP_001338271.1:n.-279+1007C>G
NM_001351343.2:c.-387+823C>G	NP_001338272.1:n.-387+823C>G
NM_001351344.2:c.-387+1007C>G	NP_001338273.1:n.-387+1007C>G
NM_001351345.2:c.-58+823C>G	NP_001338274.1:n.-58+823C>G