Canonical Allele Identifier: CA415219006

Gene: IKBKG

Linked Data

• MyVariant Identifiers: chrX:g.153792536T>G (hg19) ; chrX:g.154564321T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154564321T>G , CM000685.2:g.154564321T>G	GRCh38
NC_000023.10:g.153792536T>G , CM000685.1:g.153792536T>G	GRCh37
NC_000023.9:g.153445730T>G	NCBI36
NG_009896.1:g.27078T>G , LRG_70:g.27078T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000413620.6:c.1084T>G	ENSP00000398579.2:p.Tyr362Asp
ENST00000422680.6:c.1120T>G	ENSP00000390368.3:p.Tyr374Asp
ENST00000440286.6:c.1120T>G	ENSP00000394934.2:p.Tyr374Asp
ENST00000445622.6:c.1120T>G	ENSP00000395205.2:p.Tyr374Asp
ENST00000615186.5:c.718T>G	ENSP00000479144.2:p.Tyr240Asp
ENST00000689906.1:c.967T>G	ENSP00000508630.1:p.Tyr323Asp
ENST00000692948.1:c.1177T>G	ENSP00000508773.1:p.Tyr393Asp
ENST00000594239.6:c.1120T>G MANE Select	ENSP00000471166.1:p.Tyr374Asp
ENST00000594239.5:c.1120T>G	ENSP00000471166.1:p.Tyr374Asp
ENST00000611071.4:c.1120T>G	ENSP00000479662.1:p.Tyr374Asp
ENST00000611176.4:c.823T>G	ENSP00000478616.1:p.Tyr275Asp
ENST00000612051.1:c.*1112T>G	ENSP00000480431.1:n.*1112T>G
ENST00000615874.4:c.1096T>G	ENSP00000483381.1:p.Tyr366Asp
ENST00000617207.4:c.1117T>G	ENSP00000484023.1:p.Tyr373Asp
ENST00000618670.4:c.1324T>G	ENSP00000483825.1:p.Tyr442Asp
ENST00000619941.4:c.1099T>G	ENSP00000478979.1:p.Tyr367Asp
NM_001099856.3:c.1324T>G	NP_001093326.2:p.Tyr442Asp
NM_001099857.2:c.1120T>G	NP_001093327.1:p.Tyr374Asp
NM_001145255.2:c.823T>G	NP_001138727.1:p.Tyr275Asp
NM_003639.4:c.1120T>G	NP_003630.1:p.Tyr374Asp
XM_005274760.3:c.1321T>G	XP_005274817.1:p.Tyr441Asp
XM_005274761.3:c.1321+301T>G	XP_005274818.1:n.1321+301T>G
XM_005274764.3:c.1117T>G	XP_005274821.1:p.Tyr373Asp
XM_011531203.1:c.1171T>G	XP_011529505.1:p.Tyr391Asp
XM_011531204.1:c.1120T>G	XP_011529506.1:p.Tyr374Asp
XM_011531205.1:c.1120T>G	XP_011529507.1:p.Tyr374Asp
NM_001099856.4:c.1324T>G	NP_001093326.2:p.Tyr442Asp
NM_001321396.1:c.1120T>G	NP_001308325.1:p.Tyr374Asp
NM_001321397.1:c.1117T>G	NP_001308326.1:p.Tyr373Asp
NM_001099856.6:c.1324T>G	NP_001093326.2:p.Tyr442Asp
NM_001099857.4:c.1120T>G	NP_001093327.1:p.Tyr374Asp
NM_001145255.4:c.823T>G	NP_001138727.1:p.Tyr275Asp
NM_001321396.3:c.1120T>G	NP_001308325.1:p.Tyr374Asp
NM_001321397.3:c.1117T>G	NP_001308326.1:p.Tyr373Asp
NM_001377312.1:c.1120T>G	NP_001364241.1:p.Tyr374Asp
NM_001377313.1:c.1117T>G	NP_001364242.1:p.Tyr373Asp
NM_001377314.1:c.964T>G	NP_001364243.1:p.Tyr322Asp
NM_001377315.1:c.751T>G	NP_001364244.1:p.Tyr251Asp
NR_165197.1:n.989T>G
NM_001099857.5:c.1120T>G MANE Select	NP_001093327.1:p.Tyr374Asp