Canonical Allele Identifier: CA2466734034

Gene: IKBKG

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154564361_154564362delinsGC , CM000685.2:g.154564361_154564362delinsGC	GRCh38
NC_000023.10:g.153792576_153792577delinsGC , CM000685.1:g.153792576_153792577delinsGC	GRCh37
NC_000023.9:g.153445770_153445771delinsGC	NCBI36
NG_009896.1:g.27118_27119delinsGC , LRG_70:g.27118_27119delinsGC

Transcript Alleles

HGVS	Amino-acid change
ENST00000413620.6:c.1124_1125delinsGC	ENSP00000398579.2:p.Ser375=
ENST00000422680.6:c.1160_1161delinsGC	ENSP00000390368.3:p.Ser387=
ENST00000440286.6:c.1160_1161delinsGC	ENSP00000394934.2:p.Ser387=
ENST00000445622.6:c.1160_1161delinsGC	ENSP00000395205.2:p.Ser387=
ENST00000615186.5:c.758_759delinsGC	ENSP00000479144.2:p.Ser253=
ENST00000689906.1:c.1007_1008delinsGC	ENSP00000508630.1:p.Ser336=
ENST00000692948.1:c.1217_1218delinsGC	ENSP00000508773.1:p.Ser406=
ENST00000594239.6:c.1160_1161delinsGC MANE Select	ENSP00000471166.1:p.Ser387=
ENST00000594239.5:c.1160_1161delinsGC	ENSP00000471166.1:p.Ser387=
ENST00000611071.4:c.1160_1161delinsGC	ENSP00000479662.1:p.Ser387=
ENST00000611176.4:c.863_864delinsGC	ENSP00000478616.1:p.Ser288=
ENST00000612051.1:c.*1152_*1153delinsGC	ENSP00000480431.1:n.*1152_*1153delinsGC
ENST00000615874.4:c.1136_1137delinsGC	ENSP00000483381.1:p.Ser379=
ENST00000617207.4:c.1157_1158delinsGC	ENSP00000484023.1:p.Ser386=
ENST00000618670.4:c.1364_1365delinsGC	ENSP00000483825.1:p.Ser455=
ENST00000619941.4:c.1139_1140delinsGC	ENSP00000478979.1:p.Ser380=
NM_001099856.3:c.1364_1365delinsGC	NP_001093326.2:p.Ser455=
NM_001099857.2:c.1160_1161delinsGC	NP_001093327.1:p.Ser387=
NM_001145255.2:c.863_864delinsGC	NP_001138727.1:p.Ser288=
NM_003639.4:c.1160_1161delinsGC	NP_003630.1:p.Ser387=
XM_005274760.3:c.1361_1362delinsGC	XP_005274817.1:p.Ser454=
XM_005274761.3:c.1321+341_1321+342delinsGC	XP_005274818.1:n.1321+341_1321+342delinsGC
XM_005274764.3:c.1157_1158delinsGC	XP_005274821.1:p.Ser386=
XM_011531203.1:c.1211_1212delinsGC	XP_011529505.1:p.Ser404=
XM_011531204.1:c.1160_1161delinsGC	XP_011529506.1:p.Ser387=
XM_011531205.1:c.1160_1161delinsGC	XP_011529507.1:p.Ser387=
NM_001099856.4:c.1364_1365delinsGC	NP_001093326.2:p.Ser455=
NM_001321396.1:c.1160_1161delinsGC	NP_001308325.1:p.Ser387=
NM_001321397.1:c.1157_1158delinsGC	NP_001308326.1:p.Ser386=
NM_001099856.6:c.1364_1365delinsGC	NP_001093326.2:p.Ser455=
NM_001099857.4:c.1160_1161delinsGC	NP_001093327.1:p.Ser387=
NM_001145255.4:c.863_864delinsGC	NP_001138727.1:p.Ser288=
NM_001321396.3:c.1160_1161delinsGC	NP_001308325.1:p.Ser387=
NM_001321397.3:c.1157_1158delinsGC	NP_001308326.1:p.Ser386=
NM_001377312.1:c.1160_1161delinsGC	NP_001364241.1:p.Ser387=
NM_001377313.1:c.1157_1158delinsGC	NP_001364242.1:p.Ser386=
NM_001377314.1:c.1004_1005delinsGC	NP_001364243.1:p.Ser335=
NM_001377315.1:c.791_792delinsGC	NP_001364244.1:p.Ser264=
NR_165197.1:n.1029_1030delinsGC
NM_001099857.5:c.1160_1161delinsGC MANE Select	NP_001093327.1:p.Ser387=