Canonical Allele Identifier: CA2573119317

Gene: IKBKG

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154564330_154564334del , CM000685.2:g.154564330_154564334del	GRCh38
NC_000023.10:g.153792545_153792549del , CM000685.1:g.153792545_153792549del	GRCh37
NC_000023.9:g.153445739_153445743del	NCBI36
NG_009896.1:g.27087_27091del , LRG_70:g.27087_27091del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000413620.6:c.1093_1097del	ENSP00000398579.2:p.Ser365ProfsTer16
ENST00000422680.6:c.1129_1133del	ENSP00000390368.3:p.Ser377ProfsTer16
ENST00000440286.6:c.1129_1133del	ENSP00000394934.2:p.Ser377ProfsTer16
ENST00000445622.6:c.1129_1133del	ENSP00000395205.2:p.Ser377ProfsTer16
ENST00000615186.5:c.727_731del	ENSP00000479144.2:p.Ser243ProfsTer16
ENST00000689906.1:c.976_980del	ENSP00000508630.1:p.Ser326ProfsTer16
ENST00000692948.1:c.1186_1190del	ENSP00000508773.1:p.Ser396ProfsTer16
ENST00000594239.6:c.1129_1133del MANE Select	ENSP00000471166.1:p.Ser377ProfsTer16
ENST00000594239.5:c.1129_1133del	ENSP00000471166.1:p.Ser377ProfsTer16
ENST00000611071.4:c.1129_1133del	ENSP00000479662.1:p.Ser377ProfsTer16
ENST00000611176.4:c.832_836del	ENSP00000478616.1:p.Ser278ProfsTer16
ENST00000612051.1:c.*1121_*1125del	ENSP00000480431.1:n.*1121_*1125del
ENST00000615874.4:c.1105_1109del	ENSP00000483381.1:p.Ser369ProfsTer16
ENST00000617207.4:c.1126_1130del	ENSP00000484023.1:p.Ser376ProfsTer16
ENST00000618670.4:c.1333_1337del	ENSP00000483825.1:p.Ser445ProfsTer16
ENST00000619941.4:c.1108_1112del	ENSP00000478979.1:p.Ser370ProfsTer16
NM_001099856.3:c.1333_1337del	NP_001093326.2:p.Ser445ProfsTer16
NM_001099857.2:c.1129_1133del	NP_001093327.1:p.Ser377ProfsTer16
NM_001145255.2:c.832_836del	NP_001138727.1:p.Ser278ProfsTer16
NM_003639.4:c.1129_1133del	NP_003630.1:p.Ser377ProfsTer16
XM_005274760.3:c.1330_1334del	XP_005274817.1:p.Ser444ProfsTer16
XM_005274761.3:c.1321+310_1321+314del	XP_005274818.1:n.1321+310_1321+314del
XM_005274764.3:c.1126_1130del	XP_005274821.1:p.Ser376ProfsTer16
XM_011531203.1:c.1180_1184del	XP_011529505.1:p.Ser394ProfsTer16
XM_011531204.1:c.1129_1133del	XP_011529506.1:p.Ser377ProfsTer16
XM_011531205.1:c.1129_1133del	XP_011529507.1:p.Ser377ProfsTer16
NM_001099856.4:c.1333_1337del	NP_001093326.2:p.Ser445ProfsTer16
NM_001321396.1:c.1129_1133del	NP_001308325.1:p.Ser377ProfsTer16
NM_001321397.1:c.1126_1130del	NP_001308326.1:p.Ser376ProfsTer16
NM_001099856.6:c.1333_1337del	NP_001093326.2:p.Ser445ProfsTer16
NM_001099857.4:c.1129_1133del	NP_001093327.1:p.Ser377ProfsTer16
NM_001145255.4:c.832_836del	NP_001138727.1:p.Ser278ProfsTer16
NM_001321396.3:c.1129_1133del	NP_001308325.1:p.Ser377ProfsTer16
NM_001321397.3:c.1126_1130del	NP_001308326.1:p.Ser376ProfsTer16
NM_001377312.1:c.1129_1133del	NP_001364241.1:p.Ser377ProfsTer16
NM_001377313.1:c.1126_1130del	NP_001364242.1:p.Ser376ProfsTer16
NM_001377314.1:c.973_977del	NP_001364243.1:p.Ser325ProfsTer16
NM_001377315.1:c.760_764del	NP_001364244.1:p.Ser254ProfsTer16
NR_165197.1:n.998_1002del
NM_001099857.5:c.1129_1133del MANE Select	NP_001093327.1:p.Ser377ProfsTer16