Canonical Allele Identifier: CA3038935607
Gene: NFKBIA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.35404616del , CM000676.2:g.35404616del GRCh38
NC_000014.8:g.35873822del , CM000676.1:g.35873822del GRCh37
NC_000014.7:g.34943573del NCBI36
NG_007571.1:g.5123del , LRG_89:g.5123del

Transcript Alleles

HGVS Amino-acid Change
ENST00000553342.2:c.29del ENSP00000451281.2:p.Glu10GlyfsTer11
ENST00000557459.2:n.127del
ENST00000697957.1:n.134del
ENST00000697958.1:n.127del
ENST00000697959.1:n.134del
ENST00000697960.1:n.114del
ENST00000697961.1:c.29del ENSP00000513487.1:p.Glu10GlyfsTer11
ENST00000697966.1:n.49-2del
ENST00000216797.10:c.29del MANE Select ENSP00000216797.6:p.Glu10GlyfsTer11
ENST00000216797.9:c.29del ENSP00000216797.5:p.Glu10GlyfsTer11
ENST00000553342.1:c.29del ENSP00000451281.1:p.Glu10GlyfsTer11
ENST00000554001.5:c.29del ENSP00000450537.1:p.Glu10GlyfsTer11
ENST00000555629.1:n.134del
ENST00000557100.5:n.85del
ENST00000557140.5:c.29del ENSP00000451257.1:p.Glu10GlyfsTer11
ENST00000557459.1:n.127del
NM_020529.2:c.29del , LRG_89t1:c.29del NP_065390.1:p.Glu10GlyfsTer11
NM_020529.3:c.29del MANE Select NP_065390.1:p.Glu10GlyfsTer11