Canonical Allele Identifier: CA519286297

Gene: IKBKG

Linked Data

• MyVariant Identifiers: chrX:g.153789993G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154561778G>A , CM000685.2:g.154561778G>A	GRCh38
NC_000023.10:g.153789993G>A , CM000685.1:g.153789993G>A	GRCh37
NC_000023.9:g.153443187G>A	NCBI36
NG_009896.1:g.24535G>A , LRG_70:g.24535G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000413620.6:c.726G>A	ENSP00000398579.2:p.Arg242=
ENST00000422680.6:c.762G>A	ENSP00000390368.3:p.Arg254=
ENST00000440286.6:c.762G>A	ENSP00000394934.2:p.Arg254=
ENST00000445622.6:c.762G>A	ENSP00000395205.2:p.Arg254=
ENST00000615186.5:c.360G>A	ENSP00000479144.2:p.Arg120=
ENST00000686774.1:c.*143G>A	ENSP00000510218.1:n.*143G>A
ENST00000687445.1:n.1134G>A
ENST00000689906.1:c.609G>A	ENSP00000508630.1:p.Arg203=
ENST00000692948.1:c.819G>A	ENSP00000508773.1:p.Arg273=
ENST00000693029.1:n.1137G>A
ENST00000594239.6:c.762G>A MANE Select	ENSP00000471166.1:p.Arg254=
ENST00000594239.5:c.762G>A	ENSP00000471166.1:p.Arg254=
ENST00000611071.4:c.762G>A	ENSP00000479662.1:p.Arg254=
ENST00000611176.4:c.609G>A	ENSP00000478616.1:p.Arg203=
ENST00000612051.1:c.*754G>A	ENSP00000480431.1:n.*754G>A
ENST00000615874.4:c.744+15G>A	ENSP00000483381.1:n.744+15G>A
ENST00000617207.4:c.759G>A	ENSP00000484023.1:p.Arg253=
ENST00000617838.1:n.200-1032G>A
ENST00000618670.4:c.966G>A	ENSP00000483825.1:p.Arg322=
ENST00000619941.4:c.747+15G>A	ENSP00000478979.1:n.747+15G>A
NM_001099856.3:c.966G>A	NP_001093326.2:p.Arg322=
NM_001099857.2:c.762G>A	NP_001093327.1:p.Arg254=
NM_001145255.2:c.609G>A	NP_001138727.1:p.Arg203=
NM_003639.4:c.762G>A	NP_003630.1:p.Arg254=
XM_005274760.3:c.963G>A	XP_005274817.1:p.Arg321=
XM_005274761.3:c.966G>A	XP_005274818.1:p.Arg322=
XM_005274764.3:c.759G>A	XP_005274821.1:p.Arg253=
XM_011531203.1:c.813G>A	XP_011529505.1:p.Arg271=
XM_011531204.1:c.762G>A	XP_011529506.1:p.Arg254=
XM_011531205.1:c.762G>A	XP_011529507.1:p.Arg254=
NM_001099856.4:c.966G>A	NP_001093326.2:p.Arg322=
NM_001321396.1:c.762G>A	NP_001308325.1:p.Arg254=
NM_001321397.1:c.759G>A	NP_001308326.1:p.Arg253=
NM_001099856.6:c.966G>A	NP_001093326.2:p.Arg322=
NM_001099857.4:c.762G>A	NP_001093327.1:p.Arg254=
NM_001145255.4:c.609G>A	NP_001138727.1:p.Arg203=
NM_001321396.3:c.762G>A	NP_001308325.1:p.Arg254=
NM_001321397.3:c.759G>A	NP_001308326.1:p.Arg253=
NM_001377312.1:c.762G>A	NP_001364241.1:p.Arg254=
NM_001377313.1:c.759G>A	NP_001364242.1:p.Arg253=
NM_001377314.1:c.606G>A	NP_001364243.1:p.Arg202=
NM_001377315.1:c.400-1032G>A	NP_001364244.1:n.400-1032G>A
NR_165197.1:n.631G>A
NM_001099857.5:c.762G>A MANE Select	NP_001093327.1:p.Arg254=