Canonical Allele Identifier: CA415219367

Gene: IKBKG

Linked Data

• MyVariant Identifiers: chrX:g.153792568G>T (hg19) ; chrX:g.154564353G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154564353G>T , CM000685.2:g.154564353G>T	GRCh38
NC_000023.10:g.153792568G>T , CM000685.1:g.153792568G>T	GRCh37
NC_000023.9:g.153445762G>T	NCBI36
NG_009896.1:g.27110G>T , LRG_70:g.27110G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000413620.6:c.1116G>T	ENSP00000398579.2:p.Gln372His
ENST00000422680.6:c.1152G>T	ENSP00000390368.3:p.Gln384His
ENST00000440286.6:c.1152G>T	ENSP00000394934.2:p.Gln384His
ENST00000445622.6:c.1152G>T	ENSP00000395205.2:p.Gln384His
ENST00000615186.5:c.750G>T	ENSP00000479144.2:p.Gln250His
ENST00000689906.1:c.999G>T	ENSP00000508630.1:p.Gln333His
ENST00000692948.1:c.1209G>T	ENSP00000508773.1:p.Gln403His
ENST00000594239.6:c.1152G>T MANE Select	ENSP00000471166.1:p.Gln384His
ENST00000594239.5:c.1152G>T	ENSP00000471166.1:p.Gln384His
ENST00000611071.4:c.1152G>T	ENSP00000479662.1:p.Gln384His
ENST00000611176.4:c.855G>T	ENSP00000478616.1:p.Gln285His
ENST00000612051.1:c.*1144G>T	ENSP00000480431.1:n.*1144G>T
ENST00000615874.4:c.1128G>T	ENSP00000483381.1:p.Gln376His
ENST00000617207.4:c.1149G>T	ENSP00000484023.1:p.Gln383His
ENST00000618670.4:c.1356G>T	ENSP00000483825.1:p.Gln452His
ENST00000619941.4:c.1131G>T	ENSP00000478979.1:p.Gln377His
NM_001099856.3:c.1356G>T	NP_001093326.2:p.Gln452His
NM_001099857.2:c.1152G>T	NP_001093327.1:p.Gln384His
NM_001145255.2:c.855G>T	NP_001138727.1:p.Gln285His
NM_003639.4:c.1152G>T	NP_003630.1:p.Gln384His
XM_005274760.3:c.1353G>T	XP_005274817.1:p.Gln451His
XM_005274761.3:c.1321+333G>T	XP_005274818.1:n.1321+333G>T
XM_005274764.3:c.1149G>T	XP_005274821.1:p.Gln383His
XM_011531203.1:c.1203G>T	XP_011529505.1:p.Gln401His
XM_011531204.1:c.1152G>T	XP_011529506.1:p.Gln384His
XM_011531205.1:c.1152G>T	XP_011529507.1:p.Gln384His
NM_001099856.4:c.1356G>T	NP_001093326.2:p.Gln452His
NM_001321396.1:c.1152G>T	NP_001308325.1:p.Gln384His
NM_001321397.1:c.1149G>T	NP_001308326.1:p.Gln383His
NM_001099856.6:c.1356G>T	NP_001093326.2:p.Gln452His
NM_001099857.4:c.1152G>T	NP_001093327.1:p.Gln384His
NM_001145255.4:c.855G>T	NP_001138727.1:p.Gln285His
NM_001321396.3:c.1152G>T	NP_001308325.1:p.Gln384His
NM_001321397.3:c.1149G>T	NP_001308326.1:p.Gln383His
NM_001377312.1:c.1152G>T	NP_001364241.1:p.Gln384His
NM_001377313.1:c.1149G>T	NP_001364242.1:p.Gln383His
NM_001377314.1:c.996G>T	NP_001364243.1:p.Gln332His
NM_001377315.1:c.783G>T	NP_001364244.1:p.Gln261His
NR_165197.1:n.1021G>T
NM_001099857.5:c.1152G>T MANE Select	NP_001093327.1:p.Gln384His