Canonical Allele Identifier: CA2128943060
Community Standard Title: NM_020529.3(NFKBIA):c.*2C=
Gene: NFKBIA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.35402011G= , CM000676.2:g.35402011G= GRCh38
NC_000014.8:g.35871217G= , CM000676.1:g.35871217G= GRCh37
NC_000014.7:g.34940968G= NCBI36
NG_007571.1:g.7728C= , LRG_89:g.7728C=

Transcript Alleles

HGVS Amino-acid Change
NM_020529.3:c.*2C= MANE Select NP_065390.1:n.*2C=
ENST00000216797.10:c.*2C= MANE Select ENSP00000216797.6:n.*2C=
NM_020529.2:c.*2C= , LRG_89t1:c.*2C= NP_065390.1:n.*2C=
ENST00000216797.9:c.*2C= ENSP00000216797.5:n.*2C=
ENST00000553342.2:c.*2C= ENSP00000451281.2:n.*2C=
ENST00000554001.5:c.*598C= ENSP00000450537.1:n.*598C=
ENST00000555371.1:n.605C=
ENST00000557140.5:c.*2C= ENSP00000451257.1:n.*2C=
ENST00000557389.1:c.*2C= ENSP00000450514.1:n.*2C=
ENST00000557459.2:n.1784C=
ENST00000697954.1:n.1165C=
ENST00000697955.1:n.1204C=
ENST00000697956.1:n.1232C=
ENST00000697957.1:n.1351C=
ENST00000697958.1:n.2006C=
ENST00000697959.1:n.1684C=
ENST00000697960.1:n.2100C=
ENST00000697961.1:c.*371C= ENSP00000513487.1:n.*371C=
ENST00000697962.1:c.*371C= ENSP00000513488.1:n.*371C=
ENST00000697965.1:n.164C=