Canonical Allele Identifier: CA415215550

Gene: IKBKG

Linked Data

• MyVariant Identifiers: chrX:g.153789965T>G (hg19) ; chrX:g.154561750T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154561750T>G , CM000685.2:g.154561750T>G	GRCh38
NC_000023.10:g.153789965T>G , CM000685.1:g.153789965T>G	GRCh37
NC_000023.9:g.153443159T>G	NCBI36
NG_009896.1:g.24507T>G , LRG_70:g.24507T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000413620.6:c.698T>G	ENSP00000398579.2:p.Ile233Ser
ENST00000422680.6:c.734T>G	ENSP00000390368.3:p.Ile245Ser
ENST00000440286.6:c.734T>G	ENSP00000394934.2:p.Ile245Ser
ENST00000445622.6:c.734T>G	ENSP00000395205.2:p.Ile245Ser
ENST00000615186.5:c.332T>G	ENSP00000479144.2:p.Ile111Ser
ENST00000686774.1:c.*115T>G	ENSP00000510218.1:n.*115T>G
ENST00000687445.1:n.1106T>G
ENST00000689906.1:c.581T>G	ENSP00000508630.1:p.Ile194Ser
ENST00000692948.1:c.791T>G	ENSP00000508773.1:p.Ile264Ser
ENST00000693029.1:n.1109T>G
ENST00000594239.6:c.734T>G MANE Select	ENSP00000471166.1:p.Ile245Ser
ENST00000440286.5:c.734T>G	ENSP00000394934.1:p.Ile245Ser
ENST00000594239.5:c.734T>G	ENSP00000471166.1:p.Ile245Ser
ENST00000611071.4:c.734T>G	ENSP00000479662.1:p.Ile245Ser
ENST00000611176.4:c.581T>G	ENSP00000478616.1:p.Ile194Ser
ENST00000612051.1:c.*726T>G	ENSP00000480431.1:n.*726T>G
ENST00000615186.4:c.332T>G	ENSP00000479144.1:p.Ile111Ser
ENST00000615874.4:c.731T>G	ENSP00000483381.1:p.Ile244Ser
ENST00000617207.4:c.731T>G	ENSP00000484023.1:p.Ile244Ser
ENST00000617838.1:n.200-1060T>G
ENST00000618670.4:c.938T>G	ENSP00000483825.1:p.Ile313Ser
ENST00000619941.4:c.734T>G	ENSP00000478979.1:p.Ile245Ser
NM_001099856.3:c.938T>G	NP_001093326.2:p.Ile313Ser
NM_001099857.2:c.734T>G	NP_001093327.1:p.Ile245Ser
NM_001145255.2:c.581T>G	NP_001138727.1:p.Ile194Ser
NM_003639.4:c.734T>G	NP_003630.1:p.Ile245Ser
XM_005274760.3:c.935T>G	XP_005274817.1:p.Ile312Ser
XM_005274761.3:c.938T>G	XP_005274818.1:p.Ile313Ser
XM_005274764.3:c.731T>G	XP_005274821.1:p.Ile244Ser
XM_011531203.1:c.785T>G	XP_011529505.1:p.Ile262Ser
XM_011531204.1:c.734T>G	XP_011529506.1:p.Ile245Ser
XM_011531205.1:c.734T>G	XP_011529507.1:p.Ile245Ser
NM_001099856.4:c.938T>G	NP_001093326.2:p.Ile313Ser
NM_001321396.1:c.734T>G	NP_001308325.1:p.Ile245Ser
NM_001321397.1:c.731T>G	NP_001308326.1:p.Ile244Ser
NM_001099856.6:c.938T>G	NP_001093326.2:p.Ile313Ser
NM_001099857.4:c.734T>G	NP_001093327.1:p.Ile245Ser
NM_001145255.4:c.581T>G	NP_001138727.1:p.Ile194Ser
NM_001321396.3:c.734T>G	NP_001308325.1:p.Ile245Ser
NM_001321397.3:c.731T>G	NP_001308326.1:p.Ile244Ser
NM_001377312.1:c.734T>G	NP_001364241.1:p.Ile245Ser
NM_001377313.1:c.731T>G	NP_001364242.1:p.Ile244Ser
NM_001377314.1:c.578T>G	NP_001364243.1:p.Ile193Ser
NM_001377315.1:c.400-1060T>G	NP_001364244.1:n.400-1060T>G
NR_165197.1:n.603T>G
NM_001099857.5:c.734T>G MANE Select	NP_001093327.1:p.Ile245Ser