Canonical Allele Identifier: CA2466733998

Gene: IKBKG

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154564207G= , CM000685.2:g.154564207G=	GRCh38
NC_000023.10:g.153792422G= , CM000685.1:g.153792422G=	GRCh37
NC_000023.9:g.153445616G=	NCBI36
NG_009896.1:g.26964G= , LRG_70:g.26964G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000413620.6:c.1082-112G=	ENSP00000398579.2:n.1082-112G=
ENST00000422680.6:c.1118-112G=	ENSP00000390368.3:n.1118-112G=
ENST00000440286.6:c.1118-112G=	ENSP00000394934.2:n.1118-112G=
ENST00000445622.6:c.1118-112G=	ENSP00000395205.2:n.1118-112G=
ENST00000615186.5:c.716-112G=	ENSP00000479144.2:n.716-112G=
ENST00000689906.1:c.965-112G=	ENSP00000508630.1:n.965-112G=
ENST00000692948.1:c.1175-112G=	ENSP00000508773.1:n.1175-112G=
ENST00000693029.1:n.2961G=
ENST00000594239.6:c.1118-112G= MANE Select	ENSP00000471166.1:n.1118-112G=
ENST00000594239.5:c.1118-112G=	ENSP00000471166.1:n.1118-112G=
ENST00000611071.4:c.1118-112G=	ENSP00000479662.1:n.1118-112G=
ENST00000611176.4:c.821-112G=	ENSP00000478616.1:n.821-112G=
ENST00000612051.1:c.*1110-112G=	ENSP00000480431.1:n.*1110-112G=
ENST00000615874.4:c.1094-112G=	ENSP00000483381.1:n.1094-112G=
ENST00000617207.4:c.1115-112G=	ENSP00000484023.1:n.1115-112G=
ENST00000618670.4:c.1322-112G=	ENSP00000483825.1:n.1322-112G=
ENST00000619941.4:c.1097-112G=	ENSP00000478979.1:n.1097-112G=
NM_001099856.3:c.1322-112G=	NP_001093326.2:n.1322-112G=
NM_001099857.2:c.1118-112G=	NP_001093327.1:n.1118-112G=
NM_001145255.2:c.821-112G=	NP_001138727.1:n.821-112G=
NM_003639.4:c.1118-112G=	NP_003630.1:n.1118-112G=
XM_005274760.3:c.1319-112G=	XP_005274817.1:n.1319-112G=
XM_005274761.3:c.1321+187G=	XP_005274818.1:n.1321+187G=
XM_005274764.3:c.1115-112G=	XP_005274821.1:n.1115-112G=
XM_011531203.1:c.1169-112G=	XP_011529505.1:n.1169-112G=
XM_011531204.1:c.1118-112G=	XP_011529506.1:n.1118-112G=
XM_011531205.1:c.1118-112G=	XP_011529507.1:n.1118-112G=
NM_001099856.4:c.1322-112G=	NP_001093326.2:n.1322-112G=
NM_001321396.1:c.1118-112G=	NP_001308325.1:n.1118-112G=
NM_001321397.1:c.1115-112G=	NP_001308326.1:n.1115-112G=
NM_001099856.6:c.1322-112G=	NP_001093326.2:n.1322-112G=
NM_001099857.4:c.1118-112G=	NP_001093327.1:n.1118-112G=
NM_001145255.4:c.821-112G=	NP_001138727.1:n.821-112G=
NM_001321396.3:c.1118-112G=	NP_001308325.1:n.1118-112G=
NM_001321397.3:c.1115-112G=	NP_001308326.1:n.1115-112G=
NM_001377312.1:c.1118-112G=	NP_001364241.1:n.1118-112G=
NM_001377313.1:c.1115-112G=	NP_001364242.1:n.1115-112G=
NM_001377314.1:c.962-112G=	NP_001364243.1:n.962-112G=
NM_001377315.1:c.749-112G=	NP_001364244.1:n.749-112G=
NR_165197.1:n.987-112G=
NM_001099857.5:c.1118-112G= MANE Select	NP_001093327.1:n.1118-112G=