Canonical Allele Identifier: CA415220595

Gene: IKBKG

Linked Data

• MyVariant Identifiers: chrX:g.153792675A>C (hg19) ; chrX:g.154564460A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154564460A>C , CM000685.2:g.154564460A>C	GRCh38
NC_000023.10:g.153792675A>C , CM000685.1:g.153792675A>C	GRCh37
NC_000023.9:g.153445869A>C	NCBI36
NG_009896.1:g.27217A>C , LRG_70:g.27217A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000413620.6:c.1223A>C	ENSP00000398579.2:p.Ter408Ser
ENST00000422680.6:c.1259A>C	ENSP00000390368.3:p.Ter420Ser
ENST00000440286.6:c.1259A>C	ENSP00000394934.2:p.Ter420Ser
ENST00000445622.6:c.1259A>C	ENSP00000395205.2:p.Ter420Ser
ENST00000615186.5:c.857A>C	ENSP00000479144.2:p.Ter286Ser
ENST00000689906.1:c.1106A>C	ENSP00000508630.1:p.Ter369Ser
ENST00000692948.1:c.1316A>C	ENSP00000508773.1:p.Ter439Ser
ENST00000594239.6:c.1259A>C MANE Select	ENSP00000471166.1:p.Ter420Ser
ENST00000594239.5:c.1259A>C	ENSP00000471166.1:p.Ter420Ser
ENST00000611071.4:c.1259A>C	ENSP00000479662.1:p.Ter420Ser
ENST00000611176.4:c.962A>C	ENSP00000478616.1:p.Ter321Ser
ENST00000612051.1:c.*1251A>C	ENSP00000480431.1:n.*1251A>C
ENST00000615874.4:c.1235A>C	ENSP00000483381.1:p.Ter412Ser
ENST00000617207.4:c.1256A>C	ENSP00000484023.1:p.Ter419Ser
ENST00000618670.4:c.1463A>C	ENSP00000483825.1:p.Ter488Ser
ENST00000619941.4:c.1238A>C	ENSP00000478979.1:p.Ter413Ser
NM_001099856.3:c.1463A>C	NP_001093326.2:p.Ter488Ser
NM_001099857.2:c.1259A>C	NP_001093327.1:p.Ter420Ser
NM_001145255.2:c.962A>C	NP_001138727.1:p.Ter321Ser
NM_003639.4:c.1259A>C	NP_003630.1:p.Ter420Ser
XM_005274760.3:c.1460A>C	XP_005274817.1:p.Ter487Ser
XM_005274761.3:c.1321+440A>C	XP_005274818.1:n.1321+440A>C
XM_005274764.3:c.1256A>C	XP_005274821.1:p.Ter419Ser
XM_011531203.1:c.1310A>C	XP_011529505.1:p.Ter437Ser
XM_011531204.1:c.1259A>C	XP_011529506.1:p.Ter420Ser
XM_011531205.1:c.1259A>C	XP_011529507.1:p.Ter420Ser
NM_001099856.4:c.1463A>C	NP_001093326.2:p.Ter488Ser
NM_001321396.1:c.1259A>C	NP_001308325.1:p.Ter420Ser
NM_001321397.1:c.1256A>C	NP_001308326.1:p.Ter419Ser
NM_001099856.6:c.1463A>C	NP_001093326.2:p.Ter488Ser
NM_001099857.4:c.1259A>C	NP_001093327.1:p.Ter420Ser
NM_001145255.4:c.962A>C	NP_001138727.1:p.Ter321Ser
NM_001321396.3:c.1259A>C	NP_001308325.1:p.Ter420Ser
NM_001321397.3:c.1256A>C	NP_001308326.1:p.Ter419Ser
NM_001377312.1:c.1259A>C	NP_001364241.1:p.Ter420Ser
NM_001377313.1:c.1256A>C	NP_001364242.1:p.Ter419Ser
NM_001377314.1:c.1103A>C	NP_001364243.1:p.Ter368Ser
NM_001377315.1:c.890A>C	NP_001364244.1:p.Ter297Ser
NR_165197.1:n.1128A>C
NM_001099857.5:c.1259A>C MANE Select	NP_001093327.1:p.Ter420Ser