Canonical Allele Identifier: CA2695237095

Gene: IKBKG

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154564435_154564436insC , CM000685.2:g.154564435_154564436insC	GRCh38
NC_000023.10:g.153792650_153792651insC , CM000685.1:g.153792650_153792651insC	GRCh37
NC_000023.9:g.153445844_153445845insC	NCBI36
NG_009896.1:g.27192_27193insC , LRG_70:g.27192_27193insC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000413620.6:c.1198_1199insC	ENSP00000398579.2:p.Ile400ThrfsTer8
ENST00000422680.6:c.1234_1235insC	ENSP00000390368.3:p.Ile412ThrfsTer8
ENST00000440286.6:c.1234_1235insC	ENSP00000394934.2:p.Ile412ThrfsTer8
ENST00000445622.6:c.1234_1235insC	ENSP00000395205.2:p.Ile412ThrfsTer8
ENST00000615186.5:c.832_833insC	ENSP00000479144.2:p.Ile278ThrfsTer8
ENST00000689906.1:c.1081_1082insC	ENSP00000508630.1:p.Ile361ThrfsTer8
ENST00000692948.1:c.1291_1292insC	ENSP00000508773.1:p.Ile431ThrfsTer8
ENST00000594239.6:c.1234_1235insC MANE Select	ENSP00000471166.1:p.Ile412ThrfsTer8
ENST00000594239.5:c.1234_1235insC	ENSP00000471166.1:p.Ile412ThrfsTer8
ENST00000611071.4:c.1234_1235insC	ENSP00000479662.1:p.Ile412ThrfsTer8
ENST00000611176.4:c.937_938insC	ENSP00000478616.1:p.Ile313ThrfsTer8
ENST00000612051.1:c.*1226_*1227insC	ENSP00000480431.1:n.*1226_*1227insC
ENST00000615874.4:c.1210_1211insC	ENSP00000483381.1:p.Ile404ThrfsTer8
ENST00000617207.4:c.1231_1232insC	ENSP00000484023.1:p.Ile411ThrfsTer8
ENST00000618670.4:c.1438_1439insC	ENSP00000483825.1:p.Ile480ThrfsTer8
ENST00000619941.4:c.1213_1214insC	ENSP00000478979.1:p.Ile405ThrfsTer8
NM_001099856.3:c.1438_1439insC	NP_001093326.2:p.Ile480ThrfsTer8
NM_001099857.2:c.1234_1235insC	NP_001093327.1:p.Ile412ThrfsTer8
NM_001145255.2:c.937_938insC	NP_001138727.1:p.Ile313ThrfsTer8
NM_003639.4:c.1234_1235insC	NP_003630.1:p.Ile412ThrfsTer8
XM_005274760.3:c.1435_1436insC	XP_005274817.1:p.Ile479ThrfsTer8
XM_005274761.3:c.1321+415_1321+416insC	XP_005274818.1:n.1321+415_1321+416insC
XM_005274764.3:c.1231_1232insC	XP_005274821.1:p.Ile411ThrfsTer8
XM_011531203.1:c.1285_1286insC	XP_011529505.1:p.Ile429ThrfsTer8
XM_011531204.1:c.1234_1235insC	XP_011529506.1:p.Ile412ThrfsTer8
XM_011531205.1:c.1234_1235insC	XP_011529507.1:p.Ile412ThrfsTer8
NM_001099856.4:c.1438_1439insC	NP_001093326.2:p.Ile480ThrfsTer8
NM_001321396.1:c.1234_1235insC	NP_001308325.1:p.Ile412ThrfsTer8
NM_001321397.1:c.1231_1232insC	NP_001308326.1:p.Ile411ThrfsTer8
NM_001099856.6:c.1438_1439insC	NP_001093326.2:p.Ile480ThrfsTer8
NM_001099857.4:c.1234_1235insC	NP_001093327.1:p.Ile412ThrfsTer8
NM_001145255.4:c.937_938insC	NP_001138727.1:p.Ile313ThrfsTer8
NM_001321396.3:c.1234_1235insC	NP_001308325.1:p.Ile412ThrfsTer8
NM_001321397.3:c.1231_1232insC	NP_001308326.1:p.Ile411ThrfsTer8
NM_001377312.1:c.1234_1235insC	NP_001364241.1:p.Ile412ThrfsTer8
NM_001377313.1:c.1231_1232insC	NP_001364242.1:p.Ile411ThrfsTer8
NM_001377314.1:c.1078_1079insC	NP_001364243.1:p.Ile360ThrfsTer8
NM_001377315.1:c.865_866insC	NP_001364244.1:p.Ile289ThrfsTer8
NR_165197.1:n.1103_1104insC
NM_001099857.5:c.1234_1235insC MANE Select	NP_001093327.1:p.Ile412ThrfsTer8