Canonical Allele Identifier: CA415215904

Gene: IKBKG

Linked Data

• dbSNP Id: rs1310793916
• gnomAD v3: X-154562813-A-G
• gnomAD v4: X-154562813-A-G
• MyVariant Identifiers: chrX:g.153791028A>G (hg19) ; chrX:g.154562813A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154562813A>G , CM000685.2:g.154562813A>G	GRCh38
NC_000023.10:g.153791028A>G , CM000685.1:g.153791028A>G	GRCh37
NC_000023.9:g.153444222A>G	NCBI36
NG_009896.1:g.25570A>G , LRG_70:g.25570A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000413620.6:c.736A>G	ENSP00000398579.2:p.Met246Val
ENST00000422680.6:c.772A>G	ENSP00000390368.3:p.Met258Val
ENST00000440286.6:c.772A>G	ENSP00000394934.2:p.Met258Val
ENST00000445622.6:c.772A>G	ENSP00000395205.2:p.Met258Val
ENST00000615186.5:c.370A>G	ENSP00000479144.2:p.Met124Val
ENST00000686774.1:c.*153A>G	ENSP00000510218.1:n.*153A>G
ENST00000687445.1:n.2169A>G
ENST00000689906.1:c.619A>G	ENSP00000508630.1:p.Met207Val
ENST00000692948.1:c.829A>G	ENSP00000508773.1:p.Met277Val
ENST00000693029.1:n.2172A>G
ENST00000594239.6:c.772A>G MANE Select	ENSP00000471166.1:p.Met258Val
ENST00000594239.5:c.772A>G	ENSP00000471166.1:p.Met258Val
ENST00000611071.4:c.772A>G	ENSP00000479662.1:p.Met258Val
ENST00000611176.4:c.616-746A>G	ENSP00000478616.1:n.616-746A>G
ENST00000612051.1:c.*764A>G	ENSP00000480431.1:n.*764A>G
ENST00000615874.4:c.748A>G	ENSP00000483381.1:p.Met250Val
ENST00000617207.4:c.769A>G	ENSP00000484023.1:p.Met257Val
ENST00000617838.1:n.203A>G
ENST00000618670.4:c.976A>G	ENSP00000483825.1:p.Met326Val
ENST00000619941.4:c.751A>G	ENSP00000478979.1:p.Met251Val
NM_001099856.3:c.976A>G	NP_001093326.2:p.Met326Val
NM_001099857.2:c.772A>G	NP_001093327.1:p.Met258Val
NM_001145255.2:c.616-746A>G	NP_001138727.1:n.616-746A>G
NM_003639.4:c.772A>G	NP_003630.1:p.Met258Val
XM_005274760.3:c.973A>G	XP_005274817.1:p.Met325Val
XM_005274761.3:c.976A>G	XP_005274818.1:p.Met326Val
XM_005274764.3:c.769A>G	XP_005274821.1:p.Met257Val
XM_011531203.1:c.823A>G	XP_011529505.1:p.Met275Val
XM_011531204.1:c.772A>G	XP_011529506.1:p.Met258Val
XM_011531205.1:c.772A>G	XP_011529507.1:p.Met258Val
NM_001099856.4:c.976A>G	NP_001093326.2:p.Met326Val
NM_001321396.1:c.772A>G	NP_001308325.1:p.Met258Val
NM_001321397.1:c.769A>G	NP_001308326.1:p.Met257Val
NM_001099856.6:c.976A>G	NP_001093326.2:p.Met326Val
NM_001099857.4:c.772A>G	NP_001093327.1:p.Met258Val
NM_001145255.4:c.616-746A>G	NP_001138727.1:n.616-746A>G
NM_001321396.3:c.772A>G	NP_001308325.1:p.Met258Val
NM_001321397.3:c.769A>G	NP_001308326.1:p.Met257Val
NM_001377312.1:c.772A>G	NP_001364241.1:p.Met258Val
NM_001377313.1:c.769A>G	NP_001364242.1:p.Met257Val
NM_001377314.1:c.616A>G	NP_001364243.1:p.Met206Val
NM_001377315.1:c.403A>G	NP_001364244.1:p.Met135Val
NR_165197.1:n.641A>G
NM_001099857.5:c.772A>G MANE Select	NP_001093327.1:p.Met258Val