Canonical Allele Identifier: CA415215994

Gene: IKBKG

Linked Data

• MyVariant Identifiers: chrX:g.153791039A>T (hg19) ; chrX:g.154562824A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154562824A>T , CM000685.2:g.154562824A>T	GRCh38
NC_000023.10:g.153791039A>T , CM000685.1:g.153791039A>T	GRCh37
NC_000023.9:g.153444233A>T	NCBI36
NG_009896.1:g.25581A>T , LRG_70:g.25581A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000413620.6:c.747A>T	ENSP00000398579.2:p.Glu249Asp
ENST00000422680.6:c.783A>T	ENSP00000390368.3:p.Glu261Asp
ENST00000440286.6:c.783A>T	ENSP00000394934.2:p.Glu261Asp
ENST00000445622.6:c.783A>T	ENSP00000395205.2:p.Glu261Asp
ENST00000615186.5:c.381A>T	ENSP00000479144.2:p.Glu127Asp
ENST00000686774.1:c.*164A>T	ENSP00000510218.1:n.*164A>T
ENST00000687445.1:n.2180A>T
ENST00000689906.1:c.630A>T	ENSP00000508630.1:p.Glu210Asp
ENST00000692948.1:c.840A>T	ENSP00000508773.1:p.Glu280Asp
ENST00000693029.1:n.2183A>T
ENST00000594239.6:c.783A>T MANE Select	ENSP00000471166.1:p.Glu261Asp
ENST00000594239.5:c.783A>T	ENSP00000471166.1:p.Glu261Asp
ENST00000611071.4:c.783A>T	ENSP00000479662.1:p.Glu261Asp
ENST00000611176.4:c.616-735A>T	ENSP00000478616.1:n.616-735A>T
ENST00000612051.1:c.*775A>T	ENSP00000480431.1:n.*775A>T
ENST00000615874.4:c.759A>T	ENSP00000483381.1:p.Glu253Asp
ENST00000617207.4:c.780A>T	ENSP00000484023.1:p.Glu260Asp
ENST00000617838.1:n.214A>T
ENST00000618670.4:c.987A>T	ENSP00000483825.1:p.Glu329Asp
ENST00000619941.4:c.762A>T	ENSP00000478979.1:p.Glu254Asp
NM_001099856.3:c.987A>T	NP_001093326.2:p.Glu329Asp
NM_001099857.2:c.783A>T	NP_001093327.1:p.Glu261Asp
NM_001145255.2:c.616-735A>T	NP_001138727.1:n.616-735A>T
NM_003639.4:c.783A>T	NP_003630.1:p.Glu261Asp
XM_005274760.3:c.984A>T	XP_005274817.1:p.Glu328Asp
XM_005274761.3:c.987A>T	XP_005274818.1:p.Glu329Asp
XM_005274764.3:c.780A>T	XP_005274821.1:p.Glu260Asp
XM_011531203.1:c.834A>T	XP_011529505.1:p.Glu278Asp
XM_011531204.1:c.783A>T	XP_011529506.1:p.Glu261Asp
XM_011531205.1:c.783A>T	XP_011529507.1:p.Glu261Asp
NM_001099856.4:c.987A>T	NP_001093326.2:p.Glu329Asp
NM_001321396.1:c.783A>T	NP_001308325.1:p.Glu261Asp
NM_001321397.1:c.780A>T	NP_001308326.1:p.Glu260Asp
NM_001099856.6:c.987A>T	NP_001093326.2:p.Glu329Asp
NM_001099857.4:c.783A>T	NP_001093327.1:p.Glu261Asp
NM_001145255.4:c.616-735A>T	NP_001138727.1:n.616-735A>T
NM_001321396.3:c.783A>T	NP_001308325.1:p.Glu261Asp
NM_001321397.3:c.780A>T	NP_001308326.1:p.Glu260Asp
NM_001377312.1:c.783A>T	NP_001364241.1:p.Glu261Asp
NM_001377313.1:c.780A>T	NP_001364242.1:p.Glu260Asp
NM_001377314.1:c.627A>T	NP_001364243.1:p.Glu209Asp
NM_001377315.1:c.414A>T	NP_001364244.1:p.Glu138Asp
NR_165197.1:n.652A>T
NM_001099857.5:c.783A>T MANE Select	NP_001093327.1:p.Glu261Asp