Canonical Allele Identifier: CA16618642
Gene: IKBKB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.42306377A>G , CM000670.2:g.42306377A>G GRCh38
NC_000008.10:g.42163895A>G , CM000670.1:g.42163895A>G GRCh37
NC_000008.9:g.42283052A>G NCBI36
NG_041793.1:g.40076A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000416505.7:c.300A>G
ENST00000520810.6:c.512A>G MANE Select ENSP00000430684.1:p.Lys171Arg
ENST00000520835.7:c.320A>G ENSP00000430868.2:p.Lys107Arg
ENST00000629753.2:c.*326A>G ENSP00000486961.2:n.*326A>G
ENST00000648136.2:n.276A>G
ENST00000649612.3:c.276A>G
ENST00000676525.1:c.239A>G ENSP00000503997.1:p.Lys80Arg
ENST00000342222.6:c.*73A>G ENSP00000339151.2:n.*73A>G
ENST00000416505.5:c.335A>G ENSP00000404920.2:p.Lys112Arg
ENST00000517388.5:c.*245A>G ENSP00000429924.1:n.*245A>G
ENST00000517890.5:c.*270A>G ENSP00000428799.1:n.*270A>G
ENST00000517917.5:n.398A>G
ENST00000518647.5:n.610A>G
ENST00000518679.5:c.106-7945A>G ENSP00000430557.1:n.106-7945A>G
ENST00000519733.5:c.*48A>G ENSP00000429319.1:n.*48A>G
ENST00000519735.5:c.512A>G ENSP00000430483.1:p.Lys171Arg
ENST00000520201.5:n.516A>G
ENST00000520655.5:c.512A>G ENSP00000428922.1:p.Lys171Arg
ENST00000520810.5:c.512A>G ENSP00000430684.1:p.Lys171Arg
ENST00000520835.5:c.506A>G ENSP00000430868.1:p.Lys169Arg
ENST00000521661.5:c.512A>G ENSP00000428186.1:p.Lys171Arg
ENST00000522147.4:c.106-24830A>G ENSP00000428892.1:n.106-24830A>G
ENST00000523105.5:c.*270A>G ENSP00000429239.1:n.*270A>G
ENST00000523517.5:c.512A>G ENSP00000430114.1:p.Lys171Arg
ENST00000629753.1:c.512A>G ENSP00000486961.1:p.Lys171Arg
NM_001190720.2:c.506A>G NP_001177649.1:p.Lys169Arg
NM_001242778.1:c.335A>G NP_001229707.1:p.Lys112Arg
NM_001556.2:c.512A>G NP_001547.1:p.Lys171Arg
NR_033818.1:n.754A>G
NR_033819.1:n.698A>G
NR_040009.1:n.698A>G
XM_005273490.1:c.512A>G XP_005273547.1:p.Lys171Arg
XM_005273491.3:c.335A>G XP_005273548.1:p.Lys112Arg
XM_005273492.2:c.512A>G XP_005273549.1:p.Lys171Arg
XM_005273493.2:c.197A>G XP_005273550.1:p.Lys66Arg
XM_005273494.1:c.512A>G XP_005273551.1:p.Lys171Arg
XM_005273495.1:c.7A>G XP_005273552.1:p.Arg3Gly
XM_005273496.2:c.7A>G XP_005273553.1:p.Arg3Gly
XM_005273498.2:c.7A>G XP_005273555.1:p.Arg3Gly
XM_011544517.1:c.512A>G XP_011542819.1:p.Lys171Arg
XM_011544518.1:c.487A>G XP_011542820.1:p.Arg163Gly
XM_011544519.1:c.335A>G XP_011542821.1:p.Lys112Arg
XM_011544520.1:c.257A>G XP_011542822.1:p.Lys86Arg
XM_011544521.1:c.7A>G XP_011542823.1:p.Arg3Gly
XM_011544522.1:c.-326A>G XP_011542824.1:n.-326A>G
XR_949402.1:n.598A>G
NM_001556.3:c.512A>G MANE Select NP_001547.1:p.Lys171Arg
XM_005273490.3:c.512A>G XP_005273547.1:p.Lys171Arg
XM_005273491.5:c.335A>G XP_005273548.1:p.Lys112Arg
XM_005273492.4:c.512A>G XP_005273549.1:p.Lys171Arg
XM_005273493.4:c.197A>G XP_005273550.1:p.Lys66Arg
XM_005273494.3:c.512A>G XP_005273551.1:p.Lys171Arg
XM_005273495.2:c.7A>G XP_005273552.1:p.Arg3Gly
XM_005273496.4:c.7A>G XP_005273553.1:p.Arg3Gly
XM_005273498.4:c.7A>G XP_005273555.1:p.Arg3Gly
XM_011544517.2:c.512A>G XP_011542819.1:p.Lys171Arg
XM_011544518.2:c.487A>G XP_011542820.1:p.Arg163Gly
XM_011544519.2:c.335A>G XP_011542821.1:p.Lys112Arg
XM_011544520.2:c.257A>G XP_011542822.1:p.Lys86Arg
XM_011544521.2:c.7A>G XP_011542823.1:p.Arg3Gly
XM_011544522.2:c.-326A>G XP_011542824.1:n.-326A>G
XM_017013396.1:c.-326A>G XP_016868885.1:n.-326A>G
XR_001745530.2:n.696A>G
XR_949402.3:n.1178A>G
NM_001242778.2:c.335A>G NP_001229707.1:p.Lys112Arg
NR_033818.2:n.754A>G
NR_033819.2:n.698A>G
NR_040009.2:n.698A>G
NM_001190720.3:c.320A>G NP_001177649.2:p.Lys107Arg