Canonical Allele Identifier: CA2695237093

Gene: IKBKG

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154564364_154564376del , CM000685.2:g.154564364_154564376del	GRCh38
NC_000023.10:g.153792579_153792591del , CM000685.1:g.153792579_153792591del	GRCh37
NC_000023.9:g.153445773_153445785del	NCBI36
NG_009896.1:g.27121_27133del , LRG_70:g.27121_27133del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000413620.6:c.1127_1139del	ENSP00000398579.2:p.Pro376HisfsTer?
ENST00000422680.6:c.1163_1175del	ENSP00000390368.3:p.Pro388HisfsTer?
ENST00000440286.6:c.1163_1175del	ENSP00000394934.2:p.Pro388HisfsTer?
ENST00000445622.6:c.1163_1175del	ENSP00000395205.2:p.Pro388HisfsTer?
ENST00000615186.5:c.761_773del	ENSP00000479144.2:p.Pro254HisfsTer?
ENST00000689906.1:c.1010_1022del	ENSP00000508630.1:p.Pro337HisfsTer?
ENST00000692948.1:c.1220_1232del	ENSP00000508773.1:p.Pro407HisfsTer?
ENST00000594239.6:c.1163_1175del MANE Select	ENSP00000471166.1:p.Pro388HisfsTer?
ENST00000594239.5:c.1163_1175del	ENSP00000471166.1:p.Pro388HisfsTer?
ENST00000611071.4:c.1163_1175del	ENSP00000479662.1:p.Pro388HisfsTer?
ENST00000611176.4:c.866_878del	ENSP00000478616.1:p.Pro289HisfsTer?
ENST00000612051.1:c.*1155_*1167del	ENSP00000480431.1:n.*1155_*1167del
ENST00000615874.4:c.1139_1151del	ENSP00000483381.1:p.Pro380HisfsTer?
ENST00000617207.4:c.1160_1172del	ENSP00000484023.1:p.Pro387HisfsTer?
ENST00000618670.4:c.1367_1379del	ENSP00000483825.1:p.Pro456HisfsTer?
ENST00000619941.4:c.1142_1154del	ENSP00000478979.1:p.Pro381HisfsTer?
NM_001099856.3:c.1367_1379del	NP_001093326.2:p.Pro456HisfsTer?
NM_001099857.2:c.1163_1175del	NP_001093327.1:p.Pro388HisfsTer?
NM_001145255.2:c.866_878del	NP_001138727.1:p.Pro289HisfsTer?
NM_003639.4:c.1163_1175del	NP_003630.1:p.Pro388HisfsTer?
XM_005274760.3:c.1364_1376del	XP_005274817.1:p.Pro455HisfsTer?
XM_005274761.3:c.1321+344_1321+356del	XP_005274818.1:n.1321+344_1321+356del
XM_005274764.3:c.1160_1172del	XP_005274821.1:p.Pro387HisfsTer?
XM_011531203.1:c.1214_1226del	XP_011529505.1:p.Pro405HisfsTer?
XM_011531204.1:c.1163_1175del	XP_011529506.1:p.Pro388HisfsTer?
XM_011531205.1:c.1163_1175del	XP_011529507.1:p.Pro388HisfsTer?
NM_001099856.4:c.1367_1379del	NP_001093326.2:p.Pro456HisfsTer?
NM_001321396.1:c.1163_1175del	NP_001308325.1:p.Pro388HisfsTer?
NM_001321397.1:c.1160_1172del	NP_001308326.1:p.Pro387HisfsTer?
NM_001099856.6:c.1367_1379del	NP_001093326.2:p.Pro456HisfsTer?
NM_001099857.4:c.1163_1175del	NP_001093327.1:p.Pro388HisfsTer?
NM_001145255.4:c.866_878del	NP_001138727.1:p.Pro289HisfsTer?
NM_001321396.3:c.1163_1175del	NP_001308325.1:p.Pro388HisfsTer?
NM_001321397.3:c.1160_1172del	NP_001308326.1:p.Pro387HisfsTer?
NM_001377312.1:c.1163_1175del	NP_001364241.1:p.Pro388HisfsTer?
NM_001377313.1:c.1160_1172del	NP_001364242.1:p.Pro387HisfsTer?
NM_001377314.1:c.1007_1019del	NP_001364243.1:p.Pro336HisfsTer?
NM_001377315.1:c.794_806del	NP_001364244.1:p.Pro265HisfsTer?
NR_165197.1:n.1032_1044del
NM_001099857.5:c.1163_1175del MANE Select	NP_001093327.1:p.Pro388HisfsTer?