Canonical Allele Identifier: CA2128944595
Gene: NFKBIA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.35404476G= , CM000676.2:g.35404476G= GRCh38
NC_000014.8:g.35873682G= , CM000676.1:g.35873682G= GRCh37
NC_000014.7:g.34943433G= NCBI36
NG_007571.1:g.5263C= , LRG_89:g.5263C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000553342.2:c.135+34C= ENSP00000451281.2:n.135+34C=
ENST00000557459.2:n.267C=
ENST00000697957.1:n.274C=
ENST00000697958.1:n.267C=
ENST00000697959.1:n.274C=
ENST00000697960.1:n.254C=
ENST00000697961.1:c.169C= ENSP00000513487.1:p.Gln57=
ENST00000697966.1:n.187C=
ENST00000216797.10:c.169C= MANE Select ENSP00000216797.6:p.Gln57=
ENST00000216797.9:c.169C= ENSP00000216797.5:p.Gln57=
ENST00000553342.1:c.135+34C= ENSP00000451281.1:n.135+34C=
ENST00000554001.5:c.169C= ENSP00000450537.1:p.Gln57=
ENST00000555629.1:n.274C=
ENST00000557100.5:n.225C=
ENST00000557140.5:c.169C= ENSP00000451257.1:p.Gln57=
ENST00000557459.1:n.267C=
NM_020529.2:c.169C= , LRG_89t1:c.169C= NP_065390.1:p.Gln57=
NM_020529.3:c.169C= MANE Select NP_065390.1:p.Gln57=