Canonical Allele Identifier: CA415219847
Gene: IKBKG HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154564402C>A , CM000685.2:g.154564402C>A GRCh38
NC_000023.10:g.153792617C>A , CM000685.1:g.153792617C>A GRCh37
NC_000023.9:g.153445811C>A NCBI36
NG_009896.1:g.27159C>A , LRG_70:g.27159C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000413620.6:c.1165C>A ENSP00000398579.2:p.Gln389Lys
ENST00000422680.6:c.1201C>A ENSP00000390368.3:p.Gln401Lys
ENST00000440286.6:c.1201C>A ENSP00000394934.2:p.Gln401Lys
ENST00000445622.6:c.1201C>A ENSP00000395205.2:p.Gln401Lys
ENST00000615186.5:c.799C>A ENSP00000479144.2:p.Gln267Lys
ENST00000689906.1:c.1048C>A ENSP00000508630.1:p.Gln350Lys
ENST00000692948.1:c.1258C>A ENSP00000508773.1:p.Gln420Lys
ENST00000594239.6:c.1201C>A MANE Select ENSP00000471166.1:p.Gln401Lys
ENST00000594239.5:c.1201C>A ENSP00000471166.1:p.Gln401Lys
ENST00000611071.4:c.1201C>A ENSP00000479662.1:p.Gln401Lys
ENST00000611176.4:c.904C>A ENSP00000478616.1:p.Gln302Lys
ENST00000612051.1:c.*1193C>A ENSP00000480431.1:n.*1193C>A
ENST00000615874.4:c.1177C>A ENSP00000483381.1:p.Gln393Lys
ENST00000617207.4:c.1198C>A ENSP00000484023.1:p.Gln400Lys
ENST00000618670.4:c.1405C>A ENSP00000483825.1:p.Gln469Lys
ENST00000619941.4:c.1180C>A ENSP00000478979.1:p.Gln394Lys
NM_001099856.3:c.1405C>A NP_001093326.2:p.Gln469Lys
NM_001099857.2:c.1201C>A NP_001093327.1:p.Gln401Lys
NM_001145255.2:c.904C>A NP_001138727.1:p.Gln302Lys
NM_003639.4:c.1201C>A NP_003630.1:p.Gln401Lys
XM_005274760.3:c.1402C>A XP_005274817.1:p.Gln468Lys
XM_005274761.3:c.1321+382C>A XP_005274818.1:n.1321+382C>A
XM_005274764.3:c.1198C>A XP_005274821.1:p.Gln400Lys
XM_011531203.1:c.1252C>A XP_011529505.1:p.Gln418Lys
XM_011531204.1:c.1201C>A XP_011529506.1:p.Gln401Lys
XM_011531205.1:c.1201C>A XP_011529507.1:p.Gln401Lys
NM_001099856.4:c.1405C>A NP_001093326.2:p.Gln469Lys
NM_001321396.1:c.1201C>A NP_001308325.1:p.Gln401Lys
NM_001321397.1:c.1198C>A NP_001308326.1:p.Gln400Lys
NM_001099856.6:c.1405C>A NP_001093326.2:p.Gln469Lys
NM_001099857.4:c.1201C>A NP_001093327.1:p.Gln401Lys
NM_001145255.4:c.904C>A NP_001138727.1:p.Gln302Lys
NM_001321396.3:c.1201C>A NP_001308325.1:p.Gln401Lys
NM_001321397.3:c.1198C>A NP_001308326.1:p.Gln400Lys
NM_001377312.1:c.1201C>A NP_001364241.1:p.Gln401Lys
NM_001377313.1:c.1198C>A NP_001364242.1:p.Gln400Lys
NM_001377314.1:c.1045C>A NP_001364243.1:p.Gln349Lys
NM_001377315.1:c.832C>A NP_001364244.1:p.Gln278Lys
NR_165197.1:n.1070C>A
NM_001099857.5:c.1201C>A MANE Select NP_001093327.1:p.Gln401Lys