Canonical Allele Identifier: CA16621262
Gene: IKBKG HGNC NCBI

Linked Data

ClinVar Variation Id: 419829
ClinVar RCV Id: RCV000478080
dbSNP Id: rs1064794135

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154560550del , CM000685.2:g.154560550del GRCh38
NC_000023.10:g.153788765del , CM000685.1:g.153788765del GRCh37
NC_000023.9:g.153441959del NCBI36
NG_009896.1:g.23307del , LRG_70:g.23307del

Transcript Alleles

HGVS Amino-acid change
ENST00000413620.6:c.626del ENSP00000398579.2:p.Ser209TrpfsTer?
ENST00000422680.6:c.662del ENSP00000390368.3:p.Ser221TrpfsTer?
ENST00000440286.6:c.662del ENSP00000394934.2:p.Ser221TrpfsTer?
ENST00000445622.6:c.662del ENSP00000395205.2:p.Ser221TrpfsTer?
ENST00000615186.5:c.260del ENSP00000479144.2:p.Ser87TrpfsTer?
ENST00000686774.1:c.*53-1138del ENSP00000510218.1:n.*53-1138del
ENST00000687445.1:n.1034del
ENST00000689906.1:c.519-1138del ENSP00000508630.1:n.519-1138del
ENST00000692816.1:n.1037del
ENST00000692948.1:c.719del ENSP00000508773.1:p.Ser240TrpfsTer?
ENST00000693029.1:n.1037del
ENST00000594239.6:c.662del MANE Select ENSP00000471166.1:p.Ser221TrpfsTer?
ENST00000440286.5:c.662del ENSP00000394934.1:p.Ser221TrpfsTer?
ENST00000594239.5:c.662del ENSP00000471166.1:p.Ser221TrpfsTer?
ENST00000611071.4:c.662del ENSP00000479662.1:p.Ser221TrpfsTer?
ENST00000611176.4:c.519-1138del ENSP00000478616.1:n.519-1138del
ENST00000612051.1:c.*654del ENSP00000480431.1:n.*654del
ENST00000615186.4:c.260del ENSP00000479144.1:p.Ser87TrpfsTer?
ENST00000615874.4:c.659del ENSP00000483381.1:p.Ser220TrpfsTer?
ENST00000617207.4:c.659del ENSP00000484023.1:p.Ser220TrpfsTer?
ENST00000617838.1:n.200-2260del
ENST00000618670.4:c.866del ENSP00000483825.1:p.Ser289TrpfsTer?
ENST00000619941.4:c.662del ENSP00000478979.1:p.Ser221TrpfsTer?
NM_001099856.3:c.866del NP_001093326.2:p.Ser289TrpfsTer?
NM_001099857.2:c.662del NP_001093327.1:p.Ser221TrpfsTer?
NM_001145255.2:c.519-1138del NP_001138727.1:n.519-1138del
NM_003639.4:c.662del NP_003630.1:p.Ser221TrpfsTer?
XM_005274760.3:c.863del XP_005274817.1:p.Ser288TrpfsTer?
XM_005274761.3:c.866del XP_005274818.1:p.Ser289TrpfsTer?
XM_005274764.3:c.659del XP_005274821.1:p.Ser220TrpfsTer?
XM_011531203.1:c.723-1138del XP_011529505.1:n.723-1138del
XM_011531204.1:c.662del XP_011529506.1:p.Ser221TrpfsTer?
XM_011531205.1:c.662del XP_011529507.1:p.Ser221TrpfsTer?
NM_001099856.4:c.866del NP_001093326.2:p.Ser289TrpfsTer?
NM_001321396.1:c.662del NP_001308325.1:p.Ser221TrpfsTer?
NM_001321397.1:c.659del NP_001308326.1:p.Ser220TrpfsTer?
NM_001099856.6:c.866del NP_001093326.2:p.Ser289TrpfsTer?
NM_001099857.4:c.662del NP_001093327.1:p.Ser221TrpfsTer?
NM_001145255.4:c.519-1138del NP_001138727.1:n.519-1138del
NM_001321396.3:c.662del NP_001308325.1:p.Ser221TrpfsTer?
NM_001321397.3:c.659del NP_001308326.1:p.Ser220TrpfsTer?
NM_001377312.1:c.662del NP_001364241.1:p.Ser221TrpfsTer?
NM_001377313.1:c.659del NP_001364242.1:p.Ser220TrpfsTer?
NM_001377314.1:c.516-1138del NP_001364243.1:n.516-1138del
NM_001377315.1:c.400-2260del NP_001364244.1:n.400-2260del
NR_165197.1:n.541-1138del
NM_001099857.5:c.662del MANE Select NP_001093327.1:p.Ser221TrpfsTer?