Canonical Allele Identifier: CA415215929

Gene: IKBKG

Linked Data

• MyVariant Identifiers: chrX:g.153791031C>A (hg19) ; chrX:g.154562816C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154562816C>A , CM000685.2:g.154562816C>A	GRCh38
NC_000023.10:g.153791031C>A , CM000685.1:g.153791031C>A	GRCh37
NC_000023.9:g.153444225C>A	NCBI36
NG_009896.1:g.25573C>A , LRG_70:g.25573C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000413620.6:c.739C>A	ENSP00000398579.2:p.Gln247Lys
ENST00000422680.6:c.775C>A	ENSP00000390368.3:p.Gln259Lys
ENST00000440286.6:c.775C>A	ENSP00000394934.2:p.Gln259Lys
ENST00000445622.6:c.775C>A	ENSP00000395205.2:p.Gln259Lys
ENST00000615186.5:c.373C>A	ENSP00000479144.2:p.Gln125Lys
ENST00000686774.1:c.*156C>A	ENSP00000510218.1:n.*156C>A
ENST00000687445.1:n.2172C>A
ENST00000689906.1:c.622C>A	ENSP00000508630.1:p.Gln208Lys
ENST00000692948.1:c.832C>A	ENSP00000508773.1:p.Gln278Lys
ENST00000693029.1:n.2175C>A
ENST00000594239.6:c.775C>A MANE Select	ENSP00000471166.1:p.Gln259Lys
ENST00000594239.5:c.775C>A	ENSP00000471166.1:p.Gln259Lys
ENST00000611071.4:c.775C>A	ENSP00000479662.1:p.Gln259Lys
ENST00000611176.4:c.616-743C>A	ENSP00000478616.1:n.616-743C>A
ENST00000612051.1:c.*767C>A	ENSP00000480431.1:n.*767C>A
ENST00000615874.4:c.751C>A	ENSP00000483381.1:p.Gln251Lys
ENST00000617207.4:c.772C>A	ENSP00000484023.1:p.Gln258Lys
ENST00000617838.1:n.206C>A
ENST00000618670.4:c.979C>A	ENSP00000483825.1:p.Gln327Lys
ENST00000619941.4:c.754C>A	ENSP00000478979.1:p.Gln252Lys
NM_001099856.3:c.979C>A	NP_001093326.2:p.Gln327Lys
NM_001099857.2:c.775C>A	NP_001093327.1:p.Gln259Lys
NM_001145255.2:c.616-743C>A	NP_001138727.1:n.616-743C>A
NM_003639.4:c.775C>A	NP_003630.1:p.Gln259Lys
XM_005274760.3:c.976C>A	XP_005274817.1:p.Gln326Lys
XM_005274761.3:c.979C>A	XP_005274818.1:p.Gln327Lys
XM_005274764.3:c.772C>A	XP_005274821.1:p.Gln258Lys
XM_011531203.1:c.826C>A	XP_011529505.1:p.Gln276Lys
XM_011531204.1:c.775C>A	XP_011529506.1:p.Gln259Lys
XM_011531205.1:c.775C>A	XP_011529507.1:p.Gln259Lys
NM_001099856.4:c.979C>A	NP_001093326.2:p.Gln327Lys
NM_001321396.1:c.775C>A	NP_001308325.1:p.Gln259Lys
NM_001321397.1:c.772C>A	NP_001308326.1:p.Gln258Lys
NM_001099856.6:c.979C>A	NP_001093326.2:p.Gln327Lys
NM_001099857.4:c.775C>A	NP_001093327.1:p.Gln259Lys
NM_001145255.4:c.616-743C>A	NP_001138727.1:n.616-743C>A
NM_001321396.3:c.775C>A	NP_001308325.1:p.Gln259Lys
NM_001321397.3:c.772C>A	NP_001308326.1:p.Gln258Lys
NM_001377312.1:c.775C>A	NP_001364241.1:p.Gln259Lys
NM_001377313.1:c.772C>A	NP_001364242.1:p.Gln258Lys
NM_001377314.1:c.619C>A	NP_001364243.1:p.Gln207Lys
NM_001377315.1:c.406C>A	NP_001364244.1:p.Gln136Lys
NR_165197.1:n.644C>A
NM_001099857.5:c.775C>A MANE Select	NP_001093327.1:p.Gln259Lys