Canonical Allele Identifier: CA2466734032
Gene: IKBKG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154564345C= , CM000685.2:g.154564345C= GRCh38
NC_000023.10:g.153792560C= , CM000685.1:g.153792560C= GRCh37
NC_000023.9:g.153445754C= NCBI36
NG_009896.1:g.27102C= , LRG_70:g.27102C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000413620.6:c.1108C= ENSP00000398579.2:p.Pro370=
ENST00000422680.6:c.1144C= ENSP00000390368.3:p.Pro382=
ENST00000440286.6:c.1144C= ENSP00000394934.2:p.Pro382=
ENST00000445622.6:c.1144C= ENSP00000395205.2:p.Pro382=
ENST00000615186.5:c.742C= ENSP00000479144.2:p.Pro248=
ENST00000689906.1:c.991C= ENSP00000508630.1:p.Pro331=
ENST00000692948.1:c.1201C= ENSP00000508773.1:p.Pro401=
ENST00000594239.6:c.1144C= MANE Select ENSP00000471166.1:p.Pro382=
ENST00000594239.5:c.1144C= ENSP00000471166.1:p.Pro382=
ENST00000611071.4:c.1144C= ENSP00000479662.1:p.Pro382=
ENST00000611176.4:c.847C= ENSP00000478616.1:p.Pro283=
ENST00000612051.1:c.*1136C= ENSP00000480431.1:n.*1136C=
ENST00000615874.4:c.1120C= ENSP00000483381.1:p.Pro374=
ENST00000617207.4:c.1141C= ENSP00000484023.1:p.Pro381=
ENST00000618670.4:c.1348C= ENSP00000483825.1:p.Pro450=
ENST00000619941.4:c.1123C= ENSP00000478979.1:p.Pro375=
NM_001099856.3:c.1348C= NP_001093326.2:p.Pro450=
NM_001099857.2:c.1144C= NP_001093327.1:p.Pro382=
NM_001145255.2:c.847C= NP_001138727.1:p.Pro283=
NM_003639.4:c.1144C= NP_003630.1:p.Pro382=
XM_005274760.3:c.1345C= XP_005274817.1:p.Pro449=
XM_005274761.3:c.1321+325C= XP_005274818.1:n.1321+325C=
XM_005274764.3:c.1141C= XP_005274821.1:p.Pro381=
XM_011531203.1:c.1195C= XP_011529505.1:p.Pro399=
XM_011531204.1:c.1144C= XP_011529506.1:p.Pro382=
XM_011531205.1:c.1144C= XP_011529507.1:p.Pro382=
NM_001099856.4:c.1348C= NP_001093326.2:p.Pro450=
NM_001321396.1:c.1144C= NP_001308325.1:p.Pro382=
NM_001321397.1:c.1141C= NP_001308326.1:p.Pro381=
NM_001099856.6:c.1348C= NP_001093326.2:p.Pro450=
NM_001099857.4:c.1144C= NP_001093327.1:p.Pro382=
NM_001145255.4:c.847C= NP_001138727.1:p.Pro283=
NM_001321396.3:c.1144C= NP_001308325.1:p.Pro382=
NM_001321397.3:c.1141C= NP_001308326.1:p.Pro381=
NM_001377312.1:c.1144C= NP_001364241.1:p.Pro382=
NM_001377313.1:c.1141C= NP_001364242.1:p.Pro381=
NM_001377314.1:c.988C= NP_001364243.1:p.Pro330=
NM_001377315.1:c.775C= NP_001364244.1:p.Pro259=
NR_165197.1:n.1013C=
NM_001099857.5:c.1144C= MANE Select NP_001093327.1:p.Pro382=