Canonical Allele Identifier: CA415219493

Gene: IKBKG

Linked Data

• MyVariant Identifiers: chrX:g.153792581C>G (hg19) ; chrX:g.154564366C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154564366C>G , CM000685.2:g.154564366C>G	GRCh38
NC_000023.10:g.153792581C>G , CM000685.1:g.153792581C>G	GRCh37
NC_000023.9:g.153445775C>G	NCBI36
NG_009896.1:g.27123C>G , LRG_70:g.27123C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000413620.6:c.1129C>G	ENSP00000398579.2:p.Pro377Ala
ENST00000422680.6:c.1165C>G	ENSP00000390368.3:p.Pro389Ala
ENST00000440286.6:c.1165C>G	ENSP00000394934.2:p.Pro389Ala
ENST00000445622.6:c.1165C>G	ENSP00000395205.2:p.Pro389Ala
ENST00000615186.5:c.763C>G	ENSP00000479144.2:p.Pro255Ala
ENST00000689906.1:c.1012C>G	ENSP00000508630.1:p.Pro338Ala
ENST00000692948.1:c.1222C>G	ENSP00000508773.1:p.Pro408Ala
ENST00000594239.6:c.1165C>G MANE Select	ENSP00000471166.1:p.Pro389Ala
ENST00000594239.5:c.1165C>G	ENSP00000471166.1:p.Pro389Ala
ENST00000611071.4:c.1165C>G	ENSP00000479662.1:p.Pro389Ala
ENST00000611176.4:c.868C>G	ENSP00000478616.1:p.Pro290Ala
ENST00000612051.1:c.*1157C>G	ENSP00000480431.1:n.*1157C>G
ENST00000615874.4:c.1141C>G	ENSP00000483381.1:p.Pro381Ala
ENST00000617207.4:c.1162C>G	ENSP00000484023.1:p.Pro388Ala
ENST00000618670.4:c.1369C>G	ENSP00000483825.1:p.Pro457Ala
ENST00000619941.4:c.1144C>G	ENSP00000478979.1:p.Pro382Ala
NM_001099856.3:c.1369C>G	NP_001093326.2:p.Pro457Ala
NM_001099857.2:c.1165C>G	NP_001093327.1:p.Pro389Ala
NM_001145255.2:c.868C>G	NP_001138727.1:p.Pro290Ala
NM_003639.4:c.1165C>G	NP_003630.1:p.Pro389Ala
XM_005274760.3:c.1366C>G	XP_005274817.1:p.Pro456Ala
XM_005274761.3:c.1321+346C>G	XP_005274818.1:n.1321+346C>G
XM_005274764.3:c.1162C>G	XP_005274821.1:p.Pro388Ala
XM_011531203.1:c.1216C>G	XP_011529505.1:p.Pro406Ala
XM_011531204.1:c.1165C>G	XP_011529506.1:p.Pro389Ala
XM_011531205.1:c.1165C>G	XP_011529507.1:p.Pro389Ala
NM_001099856.4:c.1369C>G	NP_001093326.2:p.Pro457Ala
NM_001321396.1:c.1165C>G	NP_001308325.1:p.Pro389Ala
NM_001321397.1:c.1162C>G	NP_001308326.1:p.Pro388Ala
NM_001099856.6:c.1369C>G	NP_001093326.2:p.Pro457Ala
NM_001099857.4:c.1165C>G	NP_001093327.1:p.Pro389Ala
NM_001145255.4:c.868C>G	NP_001138727.1:p.Pro290Ala
NM_001321396.3:c.1165C>G	NP_001308325.1:p.Pro389Ala
NM_001321397.3:c.1162C>G	NP_001308326.1:p.Pro388Ala
NM_001377312.1:c.1165C>G	NP_001364241.1:p.Pro389Ala
NM_001377313.1:c.1162C>G	NP_001364242.1:p.Pro388Ala
NM_001377314.1:c.1009C>G	NP_001364243.1:p.Pro337Ala
NM_001377315.1:c.796C>G	NP_001364244.1:p.Pro266Ala
NR_165197.1:n.1034C>G
NM_001099857.5:c.1165C>G MANE Select	NP_001093327.1:p.Pro389Ala