Canonical Allele Identifier: CA415216273

Gene: IKBKG

Linked Data

• MyVariant Identifiers: chrX:g.153791088C>G (hg19) ; chrX:g.154562873C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154562873C>G , CM000685.2:g.154562873C>G	GRCh38
NC_000023.10:g.153791088C>G , CM000685.1:g.153791088C>G	GRCh37
NC_000023.9:g.153444282C>G	NCBI36
NG_009896.1:g.25630C>G , LRG_70:g.25630C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000413620.6:c.796C>G	ENSP00000398579.2:p.Gln266Glu
ENST00000422680.6:c.832C>G	ENSP00000390368.3:p.Gln278Glu
ENST00000440286.6:c.832C>G	ENSP00000394934.2:p.Gln278Glu
ENST00000445622.6:c.832C>G	ENSP00000395205.2:p.Gln278Glu
ENST00000615186.5:c.430C>G	ENSP00000479144.2:p.Gln144Glu
ENST00000686774.1:c.*213C>G	ENSP00000510218.1:n.*213C>G
ENST00000687445.1:n.2229C>G
ENST00000689906.1:c.679C>G	ENSP00000508630.1:p.Gln227Glu
ENST00000692948.1:c.889C>G	ENSP00000508773.1:p.Gln297Glu
ENST00000693029.1:n.2232C>G
ENST00000594239.6:c.832C>G MANE Select	ENSP00000471166.1:p.Gln278Glu
ENST00000594239.5:c.832C>G	ENSP00000471166.1:p.Gln278Glu
ENST00000611071.4:c.832C>G	ENSP00000479662.1:p.Gln278Glu
ENST00000611176.4:c.616-686C>G	ENSP00000478616.1:n.616-686C>G
ENST00000612051.1:c.*824C>G	ENSP00000480431.1:n.*824C>G
ENST00000615874.4:c.808C>G	ENSP00000483381.1:p.Gln270Glu
ENST00000617207.4:c.829C>G	ENSP00000484023.1:p.Gln277Glu
ENST00000617838.1:n.263C>G
ENST00000618670.4:c.1036C>G	ENSP00000483825.1:p.Gln346Glu
ENST00000619941.4:c.811C>G	ENSP00000478979.1:p.Gln271Glu
NM_001099856.3:c.1036C>G	NP_001093326.2:p.Gln346Glu
NM_001099857.2:c.832C>G	NP_001093327.1:p.Gln278Glu
NM_001145255.2:c.616-686C>G	NP_001138727.1:n.616-686C>G
NM_003639.4:c.832C>G	NP_003630.1:p.Gln278Glu
XM_005274760.3:c.1033C>G	XP_005274817.1:p.Gln345Glu
XM_005274761.3:c.1036C>G	XP_005274818.1:p.Gln346Glu
XM_005274764.3:c.829C>G	XP_005274821.1:p.Gln277Glu
XM_011531203.1:c.883C>G	XP_011529505.1:p.Gln295Glu
XM_011531204.1:c.832C>G	XP_011529506.1:p.Gln278Glu
XM_011531205.1:c.832C>G	XP_011529507.1:p.Gln278Glu
NM_001099856.4:c.1036C>G	NP_001093326.2:p.Gln346Glu
NM_001321396.1:c.832C>G	NP_001308325.1:p.Gln278Glu
NM_001321397.1:c.829C>G	NP_001308326.1:p.Gln277Glu
NM_001099856.6:c.1036C>G	NP_001093326.2:p.Gln346Glu
NM_001099857.4:c.832C>G	NP_001093327.1:p.Gln278Glu
NM_001145255.4:c.616-686C>G	NP_001138727.1:n.616-686C>G
NM_001321396.3:c.832C>G	NP_001308325.1:p.Gln278Glu
NM_001321397.3:c.829C>G	NP_001308326.1:p.Gln277Glu
NM_001377312.1:c.832C>G	NP_001364241.1:p.Gln278Glu
NM_001377313.1:c.829C>G	NP_001364242.1:p.Gln277Glu
NM_001377314.1:c.676C>G	NP_001364243.1:p.Gln226Glu
NM_001377315.1:c.463C>G	NP_001364244.1:p.Gln155Glu
NR_165197.1:n.701C>G
NM_001099857.5:c.832C>G MANE Select	NP_001093327.1:p.Gln278Glu