Canonical Allele Identifier: CA2128944709
Gene: NFKBIA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.35404673G= , CM000676.2:g.35404673G= GRCh38
NC_000014.8:g.35873879G= , CM000676.1:g.35873879G= GRCh37
NC_000014.7:g.34943630G= NCBI36
NG_007571.1:g.5066C= , LRG_89:g.5066C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000553342.2:c.-29C= ENSP00000451281.2:n.-29C=
ENST00000557459.2:n.70C=
ENST00000697957.1:n.77C=
ENST00000697958.1:n.70C=
ENST00000697959.1:n.77C=
ENST00000697960.1:n.57C=
ENST00000697961.1:c.-29C= ENSP00000513487.1:n.-29C=
ENST00000697966.1:n.29C=
ENST00000216797.10:c.-29C= MANE Select ENSP00000216797.6:n.-29C=
ENST00000216797.9:c.-29C= ENSP00000216797.5:n.-29C=
ENST00000554001.5:c.-29C= ENSP00000450537.1:n.-29C=
ENST00000555629.1:n.77C=
ENST00000557100.5:n.28C=
ENST00000557140.5:c.-29C= ENSP00000451257.1:n.-29C=
ENST00000557459.1:n.70C=
NM_020529.2:c.-29C= , LRG_89t1:c.-29C= NP_065390.1:n.-29C=
NM_020529.3:c.-29C= MANE Select NP_065390.1:n.-29C=