Canonical Allele Identifier: CA2128944633
Gene: NFKBIA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.35404561_35404576delinsGTCGTCCAGTAGCCGC , CM000676.2:g.35404561_35404576delinsGTCGTCCAGTAGCCGC GRCh38
NC_000014.8:g.35873767_35873782delinsGTCGTCCAGTAGCCGC , CM000676.1:g.35873767_35873782delinsGTCGTCCAGTAGCCGC GRCh37
NC_000014.7:g.34943518_34943533delinsGTCGTCCAGTAGCCGC NCBI36
NG_007571.1:g.5163_5178delinsGCGGCTACTGGACGAC , LRG_89:g.5163_5178delinsGCGGCTACTGGACGAC

Transcript Alleles

HGVS Amino-acid Change
ENST00000553342.2:c.69_84delinsGCGGCTACTGGACGAC ENSP00000451281.2:p.Glu23=
ENST00000557459.2:n.167_182delinsGCGGCTACTGGACGAC
ENST00000697957.1:n.174_189delinsGCGGCTACTGGACGAC
ENST00000697958.1:n.167_182delinsGCGGCTACTGGACGAC
ENST00000697959.1:n.174_189delinsGCGGCTACTGGACGAC
ENST00000697960.1:n.154_169delinsGCGGCTACTGGACGAC
ENST00000697961.1:c.69_84delinsGCGGCTACTGGACGAC ENSP00000513487.1:p.Glu23=
ENST00000697966.1:n.87_102delinsGCGGCTACTGGACGAC
ENST00000216797.10:c.69_84delinsGCGGCTACTGGACGAC MANE Select ENSP00000216797.6:p.Glu23=
ENST00000216797.9:c.69_84delinsGCGGCTACTGGACGAC ENSP00000216797.5:p.Glu23=
ENST00000553342.1:c.69_84delinsGCGGCTACTGGACGAC ENSP00000451281.1:p.Glu23=
ENST00000554001.5:c.69_84delinsGCGGCTACTGGACGAC ENSP00000450537.1:p.Glu23=
ENST00000555629.1:n.174_189delinsGCGGCTACTGGACGAC
ENST00000557100.5:n.125_140delinsGCGGCTACTGGACGAC
ENST00000557140.5:c.69_84delinsGCGGCTACTGGACGAC ENSP00000451257.1:p.Glu23=
ENST00000557459.1:n.167_182delinsGCGGCTACTGGACGAC
NM_020529.2:c.69_84delinsGCGGCTACTGGACGAC , LRG_89t1:c.69_84delinsGCGGCTACTGGACGAC NP_065390.1:p.Glu23=
NM_020529.3:c.69_84delinsGCGGCTACTGGACGAC MANE Select NP_065390.1:p.Glu23=