Canonical Allele Identifier: CA415216611

Gene: IKBKG

Linked Data

• gnomAD v4: X-154562903-G-A
• MyVariant Identifiers: chrX:g.153791118G>A (hg19) ; chrX:g.154562903G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154562903G>A , CM000685.2:g.154562903G>A	GRCh38
NC_000023.10:g.153791118G>A , CM000685.1:g.153791118G>A	GRCh37
NC_000023.9:g.153444312G>A	NCBI36
NG_009896.1:g.25660G>A , LRG_70:g.25660G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000413620.6:c.826G>A	ENSP00000398579.2:p.Ala276Thr
ENST00000422680.6:c.862G>A	ENSP00000390368.3:p.Ala288Thr
ENST00000440286.6:c.862G>A	ENSP00000394934.2:p.Ala288Thr
ENST00000445622.6:c.862G>A	ENSP00000395205.2:p.Ala288Thr
ENST00000615186.5:c.460G>A	ENSP00000479144.2:p.Ala154Thr
ENST00000686774.1:c.*243G>A	ENSP00000510218.1:n.*243G>A
ENST00000687445.1:n.2259G>A
ENST00000689906.1:c.709G>A	ENSP00000508630.1:p.Ala237Thr
ENST00000692948.1:c.919G>A	ENSP00000508773.1:p.Ala307Thr
ENST00000693029.1:n.2262G>A
ENST00000594239.6:c.862G>A MANE Select	ENSP00000471166.1:p.Ala288Thr
ENST00000594239.5:c.862G>A	ENSP00000471166.1:p.Ala288Thr
ENST00000611071.4:c.862G>A	ENSP00000479662.1:p.Ala288Thr
ENST00000611176.4:c.616-656G>A	ENSP00000478616.1:n.616-656G>A
ENST00000612051.1:c.*854G>A	ENSP00000480431.1:n.*854G>A
ENST00000615874.4:c.838G>A	ENSP00000483381.1:p.Ala280Thr
ENST00000617207.4:c.859G>A	ENSP00000484023.1:p.Ala287Thr
ENST00000618670.4:c.1066G>A	ENSP00000483825.1:p.Ala356Thr
ENST00000619941.4:c.841G>A	ENSP00000478979.1:p.Ala281Thr
NM_001099856.3:c.1066G>A	NP_001093326.2:p.Ala356Thr
NM_001099857.2:c.862G>A	NP_001093327.1:p.Ala288Thr
NM_001145255.2:c.616-656G>A	NP_001138727.1:n.616-656G>A
NM_003639.4:c.862G>A	NP_003630.1:p.Ala288Thr
XM_005274760.3:c.1063G>A	XP_005274817.1:p.Ala355Thr
XM_005274761.3:c.1066G>A	XP_005274818.1:p.Ala356Thr
XM_005274764.3:c.859G>A	XP_005274821.1:p.Ala287Thr
XM_011531203.1:c.913G>A	XP_011529505.1:p.Ala305Thr
XM_011531204.1:c.862G>A	XP_011529506.1:p.Ala288Thr
XM_011531205.1:c.862G>A	XP_011529507.1:p.Ala288Thr
NM_001099856.4:c.1066G>A	NP_001093326.2:p.Ala356Thr
NM_001321396.1:c.862G>A	NP_001308325.1:p.Ala288Thr
NM_001321397.1:c.859G>A	NP_001308326.1:p.Ala287Thr
NM_001099856.6:c.1066G>A	NP_001093326.2:p.Ala356Thr
NM_001099857.4:c.862G>A	NP_001093327.1:p.Ala288Thr
NM_001145255.4:c.616-656G>A	NP_001138727.1:n.616-656G>A
NM_001321396.3:c.862G>A	NP_001308325.1:p.Ala288Thr
NM_001321397.3:c.859G>A	NP_001308326.1:p.Ala287Thr
NM_001377312.1:c.862G>A	NP_001364241.1:p.Ala288Thr
NM_001377313.1:c.859G>A	NP_001364242.1:p.Ala287Thr
NM_001377314.1:c.706G>A	NP_001364243.1:p.Ala236Thr
NM_001377315.1:c.493G>A	NP_001364244.1:p.Ala165Thr
NR_165197.1:n.731G>A
NM_001099857.5:c.862G>A MANE Select	NP_001093327.1:p.Ala288Thr