Canonical Allele Identifier: CA415219494

Gene: IKBKG

Linked Data

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

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid change
ENST00000413620.6:c.1129C>T	ENSP00000398579.2:p.Pro377Ser
ENST00000422680.6:c.1165C>T	ENSP00000390368.3:p.Pro389Ser
ENST00000440286.6:c.1165C>T	ENSP00000394934.2:p.Pro389Ser
ENST00000445622.6:c.1165C>T	ENSP00000395205.2:p.Pro389Ser
ENST00000615186.5:c.763C>T	ENSP00000479144.2:p.Pro255Ser
ENST00000689906.1:c.1012C>T	ENSP00000508630.1:p.Pro338Ser
ENST00000692948.1:c.1222C>T	ENSP00000508773.1:p.Pro408Ser
ENST00000594239.6:c.1165C>T MANE Select	ENSP00000471166.1:p.Pro389Ser
ENST00000594239.5:c.1165C>T	ENSP00000471166.1:p.Pro389Ser
ENST00000611071.4:c.1165C>T	ENSP00000479662.1:p.Pro389Ser
ENST00000611176.4:c.868C>T	ENSP00000478616.1:p.Pro290Ser
ENST00000612051.1:c.*1157C>T	ENSP00000480431.1:n.*1157C>T
ENST00000615874.4:c.1141C>T	ENSP00000483381.1:p.Pro381Ser
ENST00000617207.4:c.1162C>T	ENSP00000484023.1:p.Pro388Ser
ENST00000618670.4:c.1369C>T	ENSP00000483825.1:p.Pro457Ser
ENST00000619941.4:c.1144C>T	ENSP00000478979.1:p.Pro382Ser
NM_001099856.3:c.1369C>T	NP_001093326.2:p.Pro457Ser
NM_001099857.2:c.1165C>T	NP_001093327.1:p.Pro389Ser
NM_001145255.2:c.868C>T	NP_001138727.1:p.Pro290Ser
NM_003639.4:c.1165C>T	NP_003630.1:p.Pro389Ser
XM_005274760.3:c.1366C>T	XP_005274817.1:p.Pro456Ser
XM_005274761.3:c.1321+346C>T	XP_005274818.1:n.1321+346C>T
XM_005274764.3:c.1162C>T	XP_005274821.1:p.Pro388Ser
XM_011531203.1:c.1216C>T	XP_011529505.1:p.Pro406Ser
XM_011531204.1:c.1165C>T	XP_011529506.1:p.Pro389Ser
XM_011531205.1:c.1165C>T	XP_011529507.1:p.Pro389Ser
NM_001099856.4:c.1369C>T	NP_001093326.2:p.Pro457Ser
NM_001321396.1:c.1165C>T	NP_001308325.1:p.Pro389Ser
NM_001321397.1:c.1162C>T	NP_001308326.1:p.Pro388Ser
NM_001099856.6:c.1369C>T	NP_001093326.2:p.Pro457Ser
NM_001099857.4:c.1165C>T	NP_001093327.1:p.Pro389Ser
NM_001145255.4:c.868C>T	NP_001138727.1:p.Pro290Ser
NM_001321396.3:c.1165C>T	NP_001308325.1:p.Pro389Ser
NM_001321397.3:c.1162C>T	NP_001308326.1:p.Pro388Ser
NM_001377312.1:c.1165C>T	NP_001364241.1:p.Pro389Ser
NM_001377313.1:c.1162C>T	NP_001364242.1:p.Pro388Ser
NM_001377314.1:c.1009C>T	NP_001364243.1:p.Pro337Ser
NM_001377315.1:c.796C>T	NP_001364244.1:p.Pro266Ser
NR_165197.1:n.1034C>T
NM_001099857.5:c.1165C>T MANE Select	NP_001093327.1:p.Pro389Ser