Canonical Allele Identifier: CA415215803

Gene: IKBKG

Linked Data

• MyVariant Identifiers: chrX:g.153789995A>C (hg19) ; chrX:g.154561780A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154561780A>C , CM000685.2:g.154561780A>C	GRCh38
NC_000023.10:g.153789995A>C , CM000685.1:g.153789995A>C	GRCh37
NC_000023.9:g.153443189A>C	NCBI36
NG_009896.1:g.24537A>C , LRG_70:g.24537A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000413620.6:c.728A>C	ENSP00000398579.2:p.Lys243Thr
ENST00000422680.6:c.764A>C	ENSP00000390368.3:p.Lys255Thr
ENST00000440286.6:c.764A>C	ENSP00000394934.2:p.Lys255Thr
ENST00000445622.6:c.764A>C	ENSP00000395205.2:p.Lys255Thr
ENST00000615186.5:c.362A>C	ENSP00000479144.2:p.Lys121Thr
ENST00000686774.1:c.*145A>C	ENSP00000510218.1:n.*145A>C
ENST00000687445.1:n.1136A>C
ENST00000689906.1:c.611A>C	ENSP00000508630.1:p.Lys204Thr
ENST00000692948.1:c.821A>C	ENSP00000508773.1:p.Lys274Thr
ENST00000693029.1:n.1139A>C
ENST00000594239.6:c.764A>C MANE Select	ENSP00000471166.1:p.Lys255Thr
ENST00000594239.5:c.764A>C	ENSP00000471166.1:p.Lys255Thr
ENST00000611071.4:c.764A>C	ENSP00000479662.1:p.Lys255Thr
ENST00000611176.4:c.611A>C	ENSP00000478616.1:p.Lys204Thr
ENST00000612051.1:c.*756A>C	ENSP00000480431.1:n.*756A>C
ENST00000615874.4:c.744+17A>C	ENSP00000483381.1:n.744+17A>C
ENST00000617207.4:c.761A>C	ENSP00000484023.1:p.Lys254Thr
ENST00000617838.1:n.200-1030A>C
ENST00000618670.4:c.968A>C	ENSP00000483825.1:p.Lys323Thr
ENST00000619941.4:c.747+17A>C	ENSP00000478979.1:n.747+17A>C
NM_001099856.3:c.968A>C	NP_001093326.2:p.Lys323Thr
NM_001099857.2:c.764A>C	NP_001093327.1:p.Lys255Thr
NM_001145255.2:c.611A>C	NP_001138727.1:p.Lys204Thr
NM_003639.4:c.764A>C	NP_003630.1:p.Lys255Thr
XM_005274760.3:c.965A>C	XP_005274817.1:p.Lys322Thr
XM_005274761.3:c.968A>C	XP_005274818.1:p.Lys323Thr
XM_005274764.3:c.761A>C	XP_005274821.1:p.Lys254Thr
XM_011531203.1:c.815A>C	XP_011529505.1:p.Lys272Thr
XM_011531204.1:c.764A>C	XP_011529506.1:p.Lys255Thr
XM_011531205.1:c.764A>C	XP_011529507.1:p.Lys255Thr
NM_001099856.4:c.968A>C	NP_001093326.2:p.Lys323Thr
NM_001321396.1:c.764A>C	NP_001308325.1:p.Lys255Thr
NM_001321397.1:c.761A>C	NP_001308326.1:p.Lys254Thr
NM_001099856.6:c.968A>C	NP_001093326.2:p.Lys323Thr
NM_001099857.4:c.764A>C	NP_001093327.1:p.Lys255Thr
NM_001145255.4:c.611A>C	NP_001138727.1:p.Lys204Thr
NM_001321396.3:c.764A>C	NP_001308325.1:p.Lys255Thr
NM_001321397.3:c.761A>C	NP_001308326.1:p.Lys254Thr
NM_001377312.1:c.764A>C	NP_001364241.1:p.Lys255Thr
NM_001377313.1:c.761A>C	NP_001364242.1:p.Lys254Thr
NM_001377314.1:c.608A>C	NP_001364243.1:p.Lys203Thr
NM_001377315.1:c.400-1030A>C	NP_001364244.1:n.400-1030A>C
NR_165197.1:n.633A>C
NM_001099857.5:c.764A>C MANE Select	NP_001093327.1:p.Lys255Thr