Canonical Allele Identifier: CA415219892

Gene: IKBKG

Linked Data

• MyVariant Identifiers: chrX:g.153792622T>A (hg19) ; chrX:g.154564407T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154564407T>A , CM000685.2:g.154564407T>A	GRCh38
NC_000023.10:g.153792622T>A , CM000685.1:g.153792622T>A	GRCh37
NC_000023.9:g.153445816T>A	NCBI36
NG_009896.1:g.27164T>A , LRG_70:g.27164T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000413620.6:c.1170T>A	ENSP00000398579.2:p.Tyr390Ter
ENST00000422680.6:c.1206T>A	ENSP00000390368.3:p.Tyr402Ter
ENST00000440286.6:c.1206T>A	ENSP00000394934.2:p.Tyr402Ter
ENST00000445622.6:c.1206T>A	ENSP00000395205.2:p.Tyr402Ter
ENST00000615186.5:c.804T>A	ENSP00000479144.2:p.Tyr268Ter
ENST00000689906.1:c.1053T>A	ENSP00000508630.1:p.Tyr351Ter
ENST00000692948.1:c.1263T>A	ENSP00000508773.1:p.Tyr421Ter
ENST00000594239.6:c.1206T>A MANE Select	ENSP00000471166.1:p.Tyr402Ter
ENST00000594239.5:c.1206T>A	ENSP00000471166.1:p.Tyr402Ter
ENST00000611071.4:c.1206T>A	ENSP00000479662.1:p.Tyr402Ter
ENST00000611176.4:c.909T>A	ENSP00000478616.1:p.Tyr303Ter
ENST00000612051.1:c.*1198T>A	ENSP00000480431.1:n.*1198T>A
ENST00000615874.4:c.1182T>A	ENSP00000483381.1:p.Tyr394Ter
ENST00000617207.4:c.1203T>A	ENSP00000484023.1:p.Tyr401Ter
ENST00000618670.4:c.1410T>A	ENSP00000483825.1:p.Tyr470Ter
ENST00000619941.4:c.1185T>A	ENSP00000478979.1:p.Tyr395Ter
NM_001099856.3:c.1410T>A	NP_001093326.2:p.Tyr470Ter
NM_001099857.2:c.1206T>A	NP_001093327.1:p.Tyr402Ter
NM_001145255.2:c.909T>A	NP_001138727.1:p.Tyr303Ter
NM_003639.4:c.1206T>A	NP_003630.1:p.Tyr402Ter
XM_005274760.3:c.1407T>A	XP_005274817.1:p.Tyr469Ter
XM_005274761.3:c.1321+387T>A	XP_005274818.1:n.1321+387T>A
XM_005274764.3:c.1203T>A	XP_005274821.1:p.Tyr401Ter
XM_011531203.1:c.1257T>A	XP_011529505.1:p.Tyr419Ter
XM_011531204.1:c.1206T>A	XP_011529506.1:p.Tyr402Ter
XM_011531205.1:c.1206T>A	XP_011529507.1:p.Tyr402Ter
NM_001099856.4:c.1410T>A	NP_001093326.2:p.Tyr470Ter
NM_001321396.1:c.1206T>A	NP_001308325.1:p.Tyr402Ter
NM_001321397.1:c.1203T>A	NP_001308326.1:p.Tyr401Ter
NM_001099856.6:c.1410T>A	NP_001093326.2:p.Tyr470Ter
NM_001099857.4:c.1206T>A	NP_001093327.1:p.Tyr402Ter
NM_001145255.4:c.909T>A	NP_001138727.1:p.Tyr303Ter
NM_001321396.3:c.1206T>A	NP_001308325.1:p.Tyr402Ter
NM_001321397.3:c.1203T>A	NP_001308326.1:p.Tyr401Ter
NM_001377312.1:c.1206T>A	NP_001364241.1:p.Tyr402Ter
NM_001377313.1:c.1203T>A	NP_001364242.1:p.Tyr401Ter
NM_001377314.1:c.1050T>A	NP_001364243.1:p.Tyr350Ter
NM_001377315.1:c.837T>A	NP_001364244.1:p.Tyr279Ter
NR_165197.1:n.1075T>A
NM_001099857.5:c.1206T>A MANE Select	NP_001093327.1:p.Tyr402Ter