Canonical Allele Identifier: CA1139532681
Gene: IKBKG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154556172_154563959del , CM000685.2:g.154556172_154563959del GRCh38

Transcript Alleles

HGVS Amino-acid Change
ENST00000413620.6:c.159_1020del
ENST00000422680.6:c.195_1056del
ENST00000440286.6:c.195_1056del
ENST00000445622.6:c.195_1056del
ENST00000615186.5:c.-87-121_654del
ENST00000687445.1:n.570_2453del
ENST00000689906.1:c.195_903del
ENST00000692948.1:c.195_1113del
ENST00000693029.1:n.570_2713del
ENST00000594239.6:c.195_1056del
ENST00000594239.5:c.195_1056del
ENST00000611071.4:c.195_1056del
ENST00000611176.4:c.195_759del
ENST00000612051.1:c.*187_*1048del
ENST00000615874.4:c.195_1032del
ENST00000617207.4:c.195_1053del
ENST00000618670.4:c.399_1260del
ENST00000619941.4:c.195_1035del
NM_001099856.3:c.399_1260del
NM_001099857.2:c.195_1056del
NM_001145255.2:c.195_759del
NM_003639.4:c.195_1056del
XM_005274760.3:c.399_1257del
XM_005274761.3:c.399_1260del
XM_005274764.3:c.195_1053del
XM_011531203.1:c.399_1107del
XM_011531204.1:c.195_1056del
XM_011531205.1:c.195_1056del
NM_001099856.4:c.399_1260del
NM_001321396.1:c.195_1056del
NM_001321397.1:c.195_1053del
NM_001099856.6:c.399_1260del
NM_001099857.4:c.195_1056del
NM_001145255.4:c.195_759del
NM_001321396.3:c.195_1056del
NM_001321397.3:c.195_1053del
NM_001377312.1:c.195_1056del
NM_001377313.1:c.195_1053del
NM_001377314.1:c.195_900del
NM_001377315.1:c.195_687del
NR_165197.1:n.336_925del
NM_001099857.5:c.195_1056del