Canonical Allele Identifier: CA519287184

Gene: IKBKG

Linked Data

• MyVariant Identifiers: chrX:g.153792595T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154564380T>G , CM000685.2:g.154564380T>G	GRCh38
NC_000023.10:g.153792595T>G , CM000685.1:g.153792595T>G	GRCh37
NC_000023.9:g.153445789T>G	NCBI36
NG_009896.1:g.27137T>G , LRG_70:g.27137T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000413620.6:c.1143T>G	ENSP00000398579.2:p.Pro381=
ENST00000422680.6:c.1179T>G	ENSP00000390368.3:p.Pro393=
ENST00000440286.6:c.1179T>G	ENSP00000394934.2:p.Pro393=
ENST00000445622.6:c.1179T>G	ENSP00000395205.2:p.Pro393=
ENST00000615186.5:c.777T>G	ENSP00000479144.2:p.Pro259=
ENST00000689906.1:c.1026T>G	ENSP00000508630.1:p.Pro342=
ENST00000692948.1:c.1236T>G	ENSP00000508773.1:p.Pro412=
ENST00000594239.6:c.1179T>G MANE Select	ENSP00000471166.1:p.Pro393=
ENST00000594239.5:c.1179T>G	ENSP00000471166.1:p.Pro393=
ENST00000611071.4:c.1179T>G	ENSP00000479662.1:p.Pro393=
ENST00000611176.4:c.882T>G	ENSP00000478616.1:p.Pro294=
ENST00000612051.1:c.*1171T>G	ENSP00000480431.1:n.*1171T>G
ENST00000615874.4:c.1155T>G	ENSP00000483381.1:p.Pro385=
ENST00000617207.4:c.1176T>G	ENSP00000484023.1:p.Pro392=
ENST00000618670.4:c.1383T>G	ENSP00000483825.1:p.Pro461=
ENST00000619941.4:c.1158T>G	ENSP00000478979.1:p.Pro386=
NM_001099856.3:c.1383T>G	NP_001093326.2:p.Pro461=
NM_001099857.2:c.1179T>G	NP_001093327.1:p.Pro393=
NM_001145255.2:c.882T>G	NP_001138727.1:p.Pro294=
NM_003639.4:c.1179T>G	NP_003630.1:p.Pro393=
XM_005274760.3:c.1380T>G	XP_005274817.1:p.Pro460=
XM_005274761.3:c.1321+360T>G	XP_005274818.1:n.1321+360T>G
XM_005274764.3:c.1176T>G	XP_005274821.1:p.Pro392=
XM_011531203.1:c.1230T>G	XP_011529505.1:p.Pro410=
XM_011531204.1:c.1179T>G	XP_011529506.1:p.Pro393=
XM_011531205.1:c.1179T>G	XP_011529507.1:p.Pro393=
NM_001099856.4:c.1383T>G	NP_001093326.2:p.Pro461=
NM_001321396.1:c.1179T>G	NP_001308325.1:p.Pro393=
NM_001321397.1:c.1176T>G	NP_001308326.1:p.Pro392=
NM_001099856.6:c.1383T>G	NP_001093326.2:p.Pro461=
NM_001099857.4:c.1179T>G	NP_001093327.1:p.Pro393=
NM_001145255.4:c.882T>G	NP_001138727.1:p.Pro294=
NM_001321396.3:c.1179T>G	NP_001308325.1:p.Pro393=
NM_001321397.3:c.1176T>G	NP_001308326.1:p.Pro392=
NM_001377312.1:c.1179T>G	NP_001364241.1:p.Pro393=
NM_001377313.1:c.1176T>G	NP_001364242.1:p.Pro392=
NM_001377314.1:c.1023T>G	NP_001364243.1:p.Pro341=
NM_001377315.1:c.810T>G	NP_001364244.1:p.Pro270=
NR_165197.1:n.1048T>G
NM_001099857.5:c.1179T>G MANE Select	NP_001093327.1:p.Pro393=