Canonical Allele Identifier: CA519286324

Gene: IKBKG

Linked Data

• MyVariant Identifiers: chrX:g.153789999A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154561784A>G , CM000685.2:g.154561784A>G	GRCh38
NC_000023.10:g.153789999A>G , CM000685.1:g.153789999A>G	GRCh37
NC_000023.9:g.153443193A>G	NCBI36
NG_009896.1:g.24541A>G , LRG_70:g.24541A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000413620.6:c.732A>G	ENSP00000398579.2:p.Arg244=
ENST00000422680.6:c.768A>G	ENSP00000390368.3:p.Arg256=
ENST00000440286.6:c.768A>G	ENSP00000394934.2:p.Arg256=
ENST00000445622.6:c.768A>G	ENSP00000395205.2:p.Arg256=
ENST00000615186.5:c.366A>G	ENSP00000479144.2:p.Arg122=
ENST00000686774.1:c.*149A>G	ENSP00000510218.1:n.*149A>G
ENST00000687445.1:n.1140A>G
ENST00000689906.1:c.615A>G	ENSP00000508630.1:p.Arg205=
ENST00000692948.1:c.825A>G	ENSP00000508773.1:p.Arg275=
ENST00000693029.1:n.1143A>G
ENST00000594239.6:c.768A>G MANE Select	ENSP00000471166.1:p.Arg256=
ENST00000594239.5:c.768A>G	ENSP00000471166.1:p.Arg256=
ENST00000611071.4:c.768A>G	ENSP00000479662.1:p.Arg256=
ENST00000611176.4:c.615A>G	ENSP00000478616.1:p.Arg205=
ENST00000612051.1:c.*760A>G	ENSP00000480431.1:n.*760A>G
ENST00000615874.4:c.744+21A>G	ENSP00000483381.1:n.744+21A>G
ENST00000617207.4:c.765A>G	ENSP00000484023.1:p.Arg255=
ENST00000617838.1:n.200-1026A>G
ENST00000618670.4:c.972A>G	ENSP00000483825.1:p.Arg324=
ENST00000619941.4:c.747+21A>G	ENSP00000478979.1:n.747+21A>G
NM_001099856.3:c.972A>G	NP_001093326.2:p.Arg324=
NM_001099857.2:c.768A>G	NP_001093327.1:p.Arg256=
NM_001145255.2:c.615A>G	NP_001138727.1:p.Arg205=
NM_003639.4:c.768A>G	NP_003630.1:p.Arg256=
XM_005274760.3:c.969A>G	XP_005274817.1:p.Arg323=
XM_005274761.3:c.972A>G	XP_005274818.1:p.Arg324=
XM_005274764.3:c.765A>G	XP_005274821.1:p.Arg255=
XM_011531203.1:c.819A>G	XP_011529505.1:p.Arg273=
XM_011531204.1:c.768A>G	XP_011529506.1:p.Arg256=
XM_011531205.1:c.768A>G	XP_011529507.1:p.Arg256=
NM_001099856.4:c.972A>G	NP_001093326.2:p.Arg324=
NM_001321396.1:c.768A>G	NP_001308325.1:p.Arg256=
NM_001321397.1:c.765A>G	NP_001308326.1:p.Arg255=
NM_001099856.6:c.972A>G	NP_001093326.2:p.Arg324=
NM_001099857.4:c.768A>G	NP_001093327.1:p.Arg256=
NM_001145255.4:c.615A>G	NP_001138727.1:p.Arg205=
NM_001321396.3:c.768A>G	NP_001308325.1:p.Arg256=
NM_001321397.3:c.765A>G	NP_001308326.1:p.Arg255=
NM_001377312.1:c.768A>G	NP_001364241.1:p.Arg256=
NM_001377313.1:c.765A>G	NP_001364242.1:p.Arg255=
NM_001377314.1:c.612A>G	NP_001364243.1:p.Arg204=
NM_001377315.1:c.400-1026A>G	NP_001364244.1:n.400-1026A>G
NR_165197.1:n.637A>G
NM_001099857.5:c.768A>G MANE Select	NP_001093327.1:p.Arg256=