Canonical Allele Identifier: CA415215154
Gene: IKBKG HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154561688G>T , CM000685.2:g.154561688G>T GRCh38
NC_000023.10:g.153789903G>T , CM000685.1:g.153789903G>T GRCh37
NC_000023.9:g.153443097G>T NCBI36
NG_009896.1:g.24445G>T , LRG_70:g.24445G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000413620.6:c.636G>T ENSP00000398579.2:p.Lys212Asn
ENST00000422680.6:c.672G>T ENSP00000390368.3:p.Lys224Asn
ENST00000440286.6:c.672G>T ENSP00000394934.2:p.Lys224Asn
ENST00000445622.6:c.672G>T ENSP00000395205.2:p.Lys224Asn
ENST00000615186.5:c.270G>T ENSP00000479144.2:p.Lys90Asn
ENST00000686774.1:c.*53G>T ENSP00000510218.1:n.*53G>T
ENST00000687445.1:n.1044G>T
ENST00000689906.1:c.519G>T ENSP00000508630.1:p.Arg173=
ENST00000692948.1:c.729G>T ENSP00000508773.1:p.Lys243Asn
ENST00000693029.1:n.1047G>T
ENST00000594239.6:c.672G>T MANE Select ENSP00000471166.1:p.Lys224Asn
ENST00000440286.5:c.672G>T ENSP00000394934.1:p.Lys224Asn
ENST00000594239.5:c.672G>T ENSP00000471166.1:p.Lys224Asn
ENST00000611071.4:c.672G>T ENSP00000479662.1:p.Lys224Asn
ENST00000611176.4:c.519G>T ENSP00000478616.1:p.Arg173=
ENST00000612051.1:c.*664G>T ENSP00000480431.1:n.*664G>T
ENST00000615186.4:c.270G>T ENSP00000479144.1:p.Lys90Asn
ENST00000615874.4:c.669G>T ENSP00000483381.1:p.Lys223Asn
ENST00000617207.4:c.669G>T ENSP00000484023.1:p.Lys223Asn
ENST00000617838.1:n.200-1122G>T
ENST00000618670.4:c.876G>T ENSP00000483825.1:p.Lys292Asn
ENST00000619941.4:c.672G>T ENSP00000478979.1:p.Lys224Asn
NM_001099856.3:c.876G>T NP_001093326.2:p.Lys292Asn
NM_001099857.2:c.672G>T NP_001093327.1:p.Lys224Asn
NM_001145255.2:c.519G>T NP_001138727.1:p.Arg173=
NM_003639.4:c.672G>T NP_003630.1:p.Lys224Asn
XM_005274760.3:c.873G>T XP_005274817.1:p.Lys291Asn
XM_005274761.3:c.876G>T XP_005274818.1:p.Lys292Asn
XM_005274764.3:c.669G>T XP_005274821.1:p.Lys223Asn
XM_011531203.1:c.723G>T XP_011529505.1:p.Arg241=
XM_011531204.1:c.672G>T XP_011529506.1:p.Lys224Asn
XM_011531205.1:c.672G>T XP_011529507.1:p.Lys224Asn
NM_001099856.4:c.876G>T NP_001093326.2:p.Lys292Asn
NM_001321396.1:c.672G>T NP_001308325.1:p.Lys224Asn
NM_001321397.1:c.669G>T NP_001308326.1:p.Lys223Asn
NM_001099856.6:c.876G>T NP_001093326.2:p.Lys292Asn
NM_001099857.4:c.672G>T NP_001093327.1:p.Lys224Asn
NM_001145255.4:c.519G>T NP_001138727.1:p.Arg173=
NM_001321396.3:c.672G>T NP_001308325.1:p.Lys224Asn
NM_001321397.3:c.669G>T NP_001308326.1:p.Lys223Asn
NM_001377312.1:c.672G>T NP_001364241.1:p.Lys224Asn
NM_001377313.1:c.669G>T NP_001364242.1:p.Lys223Asn
NM_001377314.1:c.516G>T NP_001364243.1:p.Arg172=
NM_001377315.1:c.400-1122G>T NP_001364244.1:n.400-1122G>T
NR_165197.1:n.541G>T
NM_001099857.5:c.672G>T MANE Select NP_001093327.1:p.Lys224Asn