Canonical Allele Identifier: CA2573320468

Gene: IKBKG

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154564420dup , CM000685.2:g.154564420dup	GRCh38
NC_000023.10:g.153792635dup , CM000685.1:g.153792635dup	GRCh37
NC_000023.9:g.153445829dup	NCBI36
NG_009896.1:g.27177dup , LRG_70:g.27177dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000413620.6:c.1183dup	ENSP00000398579.2:p.Met395AsnfsTer13
ENST00000422680.6:c.1219dup	ENSP00000390368.3:p.Met407AsnfsTer13
ENST00000440286.6:c.1219dup	ENSP00000394934.2:p.Met407AsnfsTer13
ENST00000445622.6:c.1219dup	ENSP00000395205.2:p.Met407AsnfsTer13
ENST00000615186.5:c.817dup	ENSP00000479144.2:p.Met273AsnfsTer13
ENST00000689906.1:c.1066dup	ENSP00000508630.1:p.Met356AsnfsTer13
ENST00000692948.1:c.1276dup	ENSP00000508773.1:p.Met426AsnfsTer13
ENST00000594239.6:c.1219dup MANE Select	ENSP00000471166.1:p.Met407AsnfsTer13
ENST00000594239.5:c.1219dup	ENSP00000471166.1:p.Met407AsnfsTer13
ENST00000611071.4:c.1219dup	ENSP00000479662.1:p.Met407AsnfsTer13
ENST00000611176.4:c.922dup	ENSP00000478616.1:p.Met308AsnfsTer13
ENST00000612051.1:c.*1211dup	ENSP00000480431.1:n.*1211dup
ENST00000615874.4:c.1195dup	ENSP00000483381.1:p.Met399AsnfsTer13
ENST00000617207.4:c.1216dup	ENSP00000484023.1:p.Met406AsnfsTer13
ENST00000618670.4:c.1423dup	ENSP00000483825.1:p.Met475AsnfsTer13
ENST00000619941.4:c.1198dup	ENSP00000478979.1:p.Met400AsnfsTer13
NM_001099856.3:c.1423dup	NP_001093326.2:p.Met475AsnfsTer13
NM_001099857.2:c.1219dup	NP_001093327.1:p.Met407AsnfsTer13
NM_001145255.2:c.922dup	NP_001138727.1:p.Met308AsnfsTer13
NM_003639.4:c.1219dup	NP_003630.1:p.Met407AsnfsTer13
XM_005274760.3:c.1420dup	XP_005274817.1:p.Met474AsnfsTer13
XM_005274761.3:c.1321+400dup	XP_005274818.1:n.1321+400dup
XM_005274764.3:c.1216dup	XP_005274821.1:p.Met406AsnfsTer13
XM_011531203.1:c.1270dup	XP_011529505.1:p.Met424AsnfsTer13
XM_011531204.1:c.1219dup	XP_011529506.1:p.Met407AsnfsTer13
XM_011531205.1:c.1219dup	XP_011529507.1:p.Met407AsnfsTer13
NM_001099856.4:c.1423dup	NP_001093326.2:p.Met475AsnfsTer13
NM_001321396.1:c.1219dup	NP_001308325.1:p.Met407AsnfsTer13
NM_001321397.1:c.1216dup	NP_001308326.1:p.Met406AsnfsTer13
NM_001099856.6:c.1423dup	NP_001093326.2:p.Met475AsnfsTer13
NM_001099857.4:c.1219dup	NP_001093327.1:p.Met407AsnfsTer13
NM_001145255.4:c.922dup	NP_001138727.1:p.Met308AsnfsTer13
NM_001321396.3:c.1219dup	NP_001308325.1:p.Met407AsnfsTer13
NM_001321397.3:c.1216dup	NP_001308326.1:p.Met406AsnfsTer13
NM_001377312.1:c.1219dup	NP_001364241.1:p.Met407AsnfsTer13
NM_001377313.1:c.1216dup	NP_001364242.1:p.Met406AsnfsTer13
NM_001377314.1:c.1063dup	NP_001364243.1:p.Met355AsnfsTer13
NM_001377315.1:c.850dup	NP_001364244.1:p.Met284AsnfsTer13
NR_165197.1:n.1088dup
NM_001099857.5:c.1219dup MANE Select	NP_001093327.1:p.Met407AsnfsTer13