Canonical Allele Identifier: CA2128944574
Gene: NFKBIA HGNC NCBI

Linked Data

dbSNP Id: rs2052766716

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.35404439_35404460del , CM000676.2:g.35404439_35404460del GRCh38
NC_000014.8:g.35873645_35873666del , CM000676.1:g.35873645_35873666del GRCh37
NC_000014.7:g.34943396_34943417del NCBI36
NG_007571.1:g.5283_5304del , LRG_89:g.5283_5304del

Transcript Alleles

HGVS Amino-acid Change
ENST00000553342.2:c.136-19_138del
ENST00000557459.2:n.287_308del
ENST00000697957.1:n.294_315del
ENST00000697958.1:n.287_308del
ENST00000697959.1:n.294_315del
ENST00000697960.1:n.274_295del
ENST00000697961.1:c.189_210del ENSP00000513487.1:p.Glu64ProfsTer19
ENST00000697966.1:n.207_228del
ENST00000216797.10:c.189_210del MANE Select ENSP00000216797.6:p.Glu64ProfsTer19
ENST00000216797.9:c.189_210del ENSP00000216797.5:p.Glu64ProfsTer19
ENST00000553342.1:c.136-19_138del
ENST00000554001.5:c.189_210del ENSP00000450537.1:p.Glu64ProfsTer21
ENST00000555629.1:n.294_315del
ENST00000557100.5:n.245_266del
ENST00000557140.5:c.189_210del ENSP00000451257.1:p.Glu64ProfsTer19
ENST00000557459.1:n.287_308del
NM_020529.2:c.189_210del , LRG_89t1:c.189_210del NP_065390.1:p.Glu64ProfsTer19
NM_020529.3:c.189_210del MANE Select NP_065390.1:p.Glu64ProfsTer19