Canonical Allele Identifier: CA519287234

Gene: IKBKG

Linked Data

• MyVariant Identifiers: chrX:g.153792634T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154564419T>C , CM000685.2:g.154564419T>C	GRCh38
NC_000023.10:g.153792634T>C , CM000685.1:g.153792634T>C	GRCh37
NC_000023.9:g.153445828T>C	NCBI36
NG_009896.1:g.27176T>C , LRG_70:g.27176T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000413620.6:c.1182T>C	ENSP00000398579.2:p.Asp394=
ENST00000422680.6:c.1218T>C	ENSP00000390368.3:p.Asp406=
ENST00000440286.6:c.1218T>C	ENSP00000394934.2:p.Asp406=
ENST00000445622.6:c.1218T>C	ENSP00000395205.2:p.Asp406=
ENST00000615186.5:c.816T>C	ENSP00000479144.2:p.Asp272=
ENST00000689906.1:c.1065T>C	ENSP00000508630.1:p.Asp355=
ENST00000692948.1:c.1275T>C	ENSP00000508773.1:p.Asp425=
ENST00000594239.6:c.1218T>C MANE Select	ENSP00000471166.1:p.Asp406=
ENST00000594239.5:c.1218T>C	ENSP00000471166.1:p.Asp406=
ENST00000611071.4:c.1218T>C	ENSP00000479662.1:p.Asp406=
ENST00000611176.4:c.921T>C	ENSP00000478616.1:p.Asp307=
ENST00000612051.1:c.*1210T>C	ENSP00000480431.1:n.*1210T>C
ENST00000615874.4:c.1194T>C	ENSP00000483381.1:p.Asp398=
ENST00000617207.4:c.1215T>C	ENSP00000484023.1:p.Asp405=
ENST00000618670.4:c.1422T>C	ENSP00000483825.1:p.Asp474=
ENST00000619941.4:c.1197T>C	ENSP00000478979.1:p.Asp399=
NM_001099856.3:c.1422T>C	NP_001093326.2:p.Asp474=
NM_001099857.2:c.1218T>C	NP_001093327.1:p.Asp406=
NM_001145255.2:c.921T>C	NP_001138727.1:p.Asp307=
NM_003639.4:c.1218T>C	NP_003630.1:p.Asp406=
XM_005274760.3:c.1419T>C	XP_005274817.1:p.Asp473=
XM_005274761.3:c.1321+399T>C	XP_005274818.1:n.1321+399T>C
XM_005274764.3:c.1215T>C	XP_005274821.1:p.Asp405=
XM_011531203.1:c.1269T>C	XP_011529505.1:p.Asp423=
XM_011531204.1:c.1218T>C	XP_011529506.1:p.Asp406=
XM_011531205.1:c.1218T>C	XP_011529507.1:p.Asp406=
NM_001099856.4:c.1422T>C	NP_001093326.2:p.Asp474=
NM_001321396.1:c.1218T>C	NP_001308325.1:p.Asp406=
NM_001321397.1:c.1215T>C	NP_001308326.1:p.Asp405=
NM_001099856.6:c.1422T>C	NP_001093326.2:p.Asp474=
NM_001099857.4:c.1218T>C	NP_001093327.1:p.Asp406=
NM_001145255.4:c.921T>C	NP_001138727.1:p.Asp307=
NM_001321396.3:c.1218T>C	NP_001308325.1:p.Asp406=
NM_001321397.3:c.1215T>C	NP_001308326.1:p.Asp405=
NM_001377312.1:c.1218T>C	NP_001364241.1:p.Asp406=
NM_001377313.1:c.1215T>C	NP_001364242.1:p.Asp405=
NM_001377314.1:c.1062T>C	NP_001364243.1:p.Asp354=
NM_001377315.1:c.849T>C	NP_001364244.1:p.Asp283=
NR_165197.1:n.1087T>C
NM_001099857.5:c.1218T>C MANE Select	NP_001093327.1:p.Asp406=