Canonical Allele Identifier: CA2466732969

Gene: IKBKG

Linked Data

• dbSNP Id: rs2071081825
• gnomAD v4: X-154558766-A-AAGACGTCGGGGC

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154558777_154558788dup , CM000685.2:g.154558777_154558788dup	GRCh38

Transcript Alleles

HGVS	Amino-acid Change
ENST00000413620.6:c.482+127_482+138dup	ENSP00000398579.2:n.482+127_482+138dup
ENST00000422680.6:c.518+127_518+138dup	ENSP00000390368.3:n.518+127_518+138dup
ENST00000440286.6:c.518+127_518+138dup	ENSP00000394934.2:n.518+127_518+138dup
ENST00000445622.6:c.518+127_518+138dup	ENSP00000395205.2:n.518+127_518+138dup
ENST00000615186.5:c.116+127_116+138dup	ENSP00000479144.2:n.116+127_116+138dup
ENST00000686774.1:c.*52+71_*52+82dup	ENSP00000510218.1:n.*52+71_*52+82dup
ENST00000687445.1:n.890+127_890+138dup
ENST00000689906.1:c.518+127_518+138dup	ENSP00000508630.1:n.518+127_518+138dup
ENST00000692816.1:n.893+127_893+138dup
ENST00000692948.1:c.518+127_518+138dup	ENSP00000508773.1:n.518+127_518+138dup
ENST00000693029.1:n.893+127_893+138dup
ENST00000594239.6:c.518+127_518+138dup MANE Select	ENSP00000471166.1:n.518+127_518+138dup
ENST00000413620.5:c.482+127_482+138dup	ENSP00000398579.1:n.482+127_482+138dup
ENST00000440286.5:c.518+127_518+138dup	ENSP00000394934.1:n.518+127_518+138dup
ENST00000594239.5:c.518+127_518+138dup	ENSP00000471166.1:n.518+127_518+138dup
ENST00000611071.4:c.518+127_518+138dup	ENSP00000479662.1:n.518+127_518+138dup
ENST00000611176.4:c.518+127_518+138dup	ENSP00000478616.1:n.518+127_518+138dup
ENST00000612051.1:c.*510+127_*510+138dup	ENSP00000480431.1:n.*510+127_*510+138dup
ENST00000615186.4:c.116+127_116+138dup	ENSP00000479144.1:n.116+127_116+138dup
ENST00000615874.4:c.515+127_515+138dup	ENSP00000483381.1:n.515+127_515+138dup
ENST00000617207.4:c.515+127_515+138dup	ENSP00000484023.1:n.515+127_515+138dup
ENST00000617838.1:n.200-4033_200-4022dup
ENST00000618670.4:c.722+127_722+138dup	ENSP00000483825.1:n.722+127_722+138dup
ENST00000619941.4:c.518+127_518+138dup	ENSP00000478979.1:n.518+127_518+138dup
NM_001099856.3:c.722+127_722+138dup	NP_001093326.2:n.722+127_722+138dup
NM_001099857.2:c.518+127_518+138dup	NP_001093327.1:n.518+127_518+138dup
NM_001145255.2:c.518+127_518+138dup	NP_001138727.1:n.518+127_518+138dup
NM_003639.4:c.518+127_518+138dup	NP_003630.1:n.518+127_518+138dup
XM_005274760.3:c.719+127_719+138dup	XP_005274817.1:n.719+127_719+138dup
XM_005274761.3:c.722+127_722+138dup	XP_005274818.1:n.722+127_722+138dup
XM_005274764.3:c.515+127_515+138dup	XP_005274821.1:n.515+127_515+138dup
XM_011531203.1:c.722+127_722+138dup	XP_011529505.1:n.722+127_722+138dup
XM_011531204.1:c.518+127_518+138dup	XP_011529506.1:n.518+127_518+138dup
XM_011531205.1:c.518+127_518+138dup	XP_011529507.1:n.518+127_518+138dup
XM_011531206.1:c.722+127_722+138dup	XP_011529508.1:n.722+127_722+138dup
XM_011531207.1:c.722+127_722+138dup	XP_011529509.1:n.722+127_722+138dup
NM_001099856.4:c.722+127_722+138dup	NP_001093326.2:n.722+127_722+138dup
NM_001321396.1:c.518+127_518+138dup	NP_001308325.1:n.518+127_518+138dup
NM_001321397.1:c.515+127_515+138dup	NP_001308326.1:n.515+127_515+138dup
NM_001099856.6:c.722+127_722+138dup	NP_001093326.2:n.722+127_722+138dup
NM_001099857.4:c.518+127_518+138dup	NP_001093327.1:n.518+127_518+138dup
NM_001145255.4:c.518+127_518+138dup	NP_001138727.1:n.518+127_518+138dup
NM_001321396.3:c.518+127_518+138dup	NP_001308325.1:n.518+127_518+138dup
NM_001321397.3:c.515+127_515+138dup	NP_001308326.1:n.515+127_515+138dup
NM_001377312.1:c.518+127_518+138dup	NP_001364241.1:n.518+127_518+138dup
NM_001377313.1:c.515+127_515+138dup	NP_001364242.1:n.515+127_515+138dup
NM_001377314.1:c.515+127_515+138dup	NP_001364243.1:n.515+127_515+138dup
NM_001377315.1:c.399+2401_399+2412dup	NP_001364244.1:n.399+2401_399+2412dup
NR_165197.1:n.540+2401_540+2412dup
NM_001099857.5:c.518+127_518+138dup MANE Select	NP_001093327.1:n.518+127_518+138dup