Canonical Allele Identifier: CA519286278

Gene: IKBKG

Linked Data

• MyVariant Identifiers: chrX:g.153789987T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154561772T>C , CM000685.2:g.154561772T>C	GRCh38
NC_000023.10:g.153789987T>C , CM000685.1:g.153789987T>C	GRCh37
NC_000023.9:g.153443181T>C	NCBI36
NG_009896.1:g.24529T>C , LRG_70:g.24529T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000413620.6:c.720T>C	ENSP00000398579.2:p.Ser240=
ENST00000422680.6:c.756T>C	ENSP00000390368.3:p.Ser252=
ENST00000440286.6:c.756T>C	ENSP00000394934.2:p.Ser252=
ENST00000445622.6:c.756T>C	ENSP00000395205.2:p.Ser252=
ENST00000615186.5:c.354T>C	ENSP00000479144.2:p.Ser118=
ENST00000686774.1:c.*137T>C	ENSP00000510218.1:n.*137T>C
ENST00000687445.1:n.1128T>C
ENST00000689906.1:c.603T>C	ENSP00000508630.1:p.Ser201=
ENST00000692948.1:c.813T>C	ENSP00000508773.1:p.Ser271=
ENST00000693029.1:n.1131T>C
ENST00000594239.6:c.756T>C MANE Select	ENSP00000471166.1:p.Ser252=
ENST00000594239.5:c.756T>C	ENSP00000471166.1:p.Ser252=
ENST00000611071.4:c.756T>C	ENSP00000479662.1:p.Ser252=
ENST00000611176.4:c.603T>C	ENSP00000478616.1:p.Ser201=
ENST00000612051.1:c.*748T>C	ENSP00000480431.1:n.*748T>C
ENST00000615874.4:c.744+9T>C	ENSP00000483381.1:n.744+9T>C
ENST00000617207.4:c.753T>C	ENSP00000484023.1:p.Ser251=
ENST00000617838.1:n.200-1038T>C
ENST00000618670.4:c.960T>C	ENSP00000483825.1:p.Ser320=
ENST00000619941.4:c.747+9T>C	ENSP00000478979.1:n.747+9T>C
NM_001099856.3:c.960T>C	NP_001093326.2:p.Ser320=
NM_001099857.2:c.756T>C	NP_001093327.1:p.Ser252=
NM_001145255.2:c.603T>C	NP_001138727.1:p.Ser201=
NM_003639.4:c.756T>C	NP_003630.1:p.Ser252=
XM_005274760.3:c.957T>C	XP_005274817.1:p.Ser319=
XM_005274761.3:c.960T>C	XP_005274818.1:p.Ser320=
XM_005274764.3:c.753T>C	XP_005274821.1:p.Ser251=
XM_011531203.1:c.807T>C	XP_011529505.1:p.Ser269=
XM_011531204.1:c.756T>C	XP_011529506.1:p.Ser252=
XM_011531205.1:c.756T>C	XP_011529507.1:p.Ser252=
NM_001099856.4:c.960T>C	NP_001093326.2:p.Ser320=
NM_001321396.1:c.756T>C	NP_001308325.1:p.Ser252=
NM_001321397.1:c.753T>C	NP_001308326.1:p.Ser251=
NM_001099856.6:c.960T>C	NP_001093326.2:p.Ser320=
NM_001099857.4:c.756T>C	NP_001093327.1:p.Ser252=
NM_001145255.4:c.603T>C	NP_001138727.1:p.Ser201=
NM_001321396.3:c.756T>C	NP_001308325.1:p.Ser252=
NM_001321397.3:c.753T>C	NP_001308326.1:p.Ser251=
NM_001377312.1:c.756T>C	NP_001364241.1:p.Ser252=
NM_001377313.1:c.753T>C	NP_001364242.1:p.Ser251=
NM_001377314.1:c.600T>C	NP_001364243.1:p.Ser200=
NM_001377315.1:c.400-1038T>C	NP_001364244.1:n.400-1038T>C
NR_165197.1:n.625T>C
NM_001099857.5:c.756T>C MANE Select	NP_001093327.1:p.Ser252=