Canonical Allele Identifier: CA519286111

Gene: IKBKG

Linked Data

• MyVariant Identifiers: chrX:g.153789939G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154561724G>A , CM000685.2:g.154561724G>A	GRCh38
NC_000023.10:g.153789939G>A , CM000685.1:g.153789939G>A	GRCh37
NC_000023.9:g.153443133G>A	NCBI36
NG_009896.1:g.24481G>A , LRG_70:g.24481G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000413620.6:c.672G>A	ENSP00000398579.2:p.Gln224=
ENST00000422680.6:c.708G>A	ENSP00000390368.3:p.Gln236=
ENST00000440286.6:c.708G>A	ENSP00000394934.2:p.Gln236=
ENST00000445622.6:c.708G>A	ENSP00000395205.2:p.Gln236=
ENST00000615186.5:c.306G>A	ENSP00000479144.2:p.Gln102=
ENST00000686774.1:c.*89G>A	ENSP00000510218.1:n.*89G>A
ENST00000687445.1:n.1080G>A
ENST00000689906.1:c.555G>A	ENSP00000508630.1:p.Gln185=
ENST00000692948.1:c.765G>A	ENSP00000508773.1:p.Gln255=
ENST00000693029.1:n.1083G>A
ENST00000594239.6:c.708G>A MANE Select	ENSP00000471166.1:p.Gln236=
ENST00000440286.5:c.708G>A	ENSP00000394934.1:p.Gln236=
ENST00000594239.5:c.708G>A	ENSP00000471166.1:p.Gln236=
ENST00000611071.4:c.708G>A	ENSP00000479662.1:p.Gln236=
ENST00000611176.4:c.555G>A	ENSP00000478616.1:p.Gln185=
ENST00000612051.1:c.*700G>A	ENSP00000480431.1:n.*700G>A
ENST00000615186.4:c.306G>A	ENSP00000479144.1:p.Gln102=
ENST00000615874.4:c.705G>A	ENSP00000483381.1:p.Gln235=
ENST00000617207.4:c.705G>A	ENSP00000484023.1:p.Gln235=
ENST00000617838.1:n.200-1086G>A
ENST00000618670.4:c.912G>A	ENSP00000483825.1:p.Gln304=
ENST00000619941.4:c.708G>A	ENSP00000478979.1:p.Gln236=
NM_001099856.3:c.912G>A	NP_001093326.2:p.Gln304=
NM_001099857.2:c.708G>A	NP_001093327.1:p.Gln236=
NM_001145255.2:c.555G>A	NP_001138727.1:p.Gln185=
NM_003639.4:c.708G>A	NP_003630.1:p.Gln236=
XM_005274760.3:c.909G>A	XP_005274817.1:p.Gln303=
XM_005274761.3:c.912G>A	XP_005274818.1:p.Gln304=
XM_005274764.3:c.705G>A	XP_005274821.1:p.Gln235=
XM_011531203.1:c.759G>A	XP_011529505.1:p.Gln253=
XM_011531204.1:c.708G>A	XP_011529506.1:p.Gln236=
XM_011531205.1:c.708G>A	XP_011529507.1:p.Gln236=
NM_001099856.4:c.912G>A	NP_001093326.2:p.Gln304=
NM_001321396.1:c.708G>A	NP_001308325.1:p.Gln236=
NM_001321397.1:c.705G>A	NP_001308326.1:p.Gln235=
NM_001099856.6:c.912G>A	NP_001093326.2:p.Gln304=
NM_001099857.4:c.708G>A	NP_001093327.1:p.Gln236=
NM_001145255.4:c.555G>A	NP_001138727.1:p.Gln185=
NM_001321396.3:c.708G>A	NP_001308325.1:p.Gln236=
NM_001321397.3:c.705G>A	NP_001308326.1:p.Gln235=
NM_001377312.1:c.708G>A	NP_001364241.1:p.Gln236=
NM_001377313.1:c.705G>A	NP_001364242.1:p.Gln235=
NM_001377314.1:c.552G>A	NP_001364243.1:p.Gln184=
NM_001377315.1:c.400-1086G>A	NP_001364244.1:n.400-1086G>A
NR_165197.1:n.577G>A
NM_001099857.5:c.708G>A MANE Select	NP_001093327.1:p.Gln236=