Canonical Allele Identifier: CA2128942831
Gene: NFKBIA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.35401604A= , CM000676.2:g.35401604A= GRCh38
NC_000014.8:g.35870810A= , CM000676.1:g.35870810A= GRCh37
NC_000014.7:g.34940561A= NCBI36
NG_007571.1:g.8135T= , LRG_89:g.8135T=

Transcript Alleles

HGVS Amino-acid change
ENST00000553342.2:c.*409T= ENSP00000451281.2:n.*409T=
ENST00000697954.1:n.1572T=
ENST00000697955.1:n.1611T=
ENST00000697956.1:n.1639T=
ENST00000697957.1:n.1758T=
ENST00000697958.1:n.2413T=
ENST00000697959.1:n.2091T=
ENST00000697960.1:n.2507T=
ENST00000697961.1:c.*778T= ENSP00000513487.1:n.*778T=
ENST00000216797.10:c.*409T= MANE Select ENSP00000216797.6:n.*409T=
ENST00000216797.9:c.*409T= ENSP00000216797.5:n.*409T=
ENST00000554001.5:c.*1005T= ENSP00000450537.1:n.*1005T=
ENST00000557140.5:c.*409T= ENSP00000451257.1:n.*409T=
ENST00000557389.1:c.*409T= ENSP00000450514.1:n.*409T=
NM_020529.2:c.*409T= , LRG_89t1:c.*409T= NP_065390.1:n.*409T=
NM_020529.3:c.*409T= MANE Select NP_065390.1:n.*409T=