Canonical Allele Identifier: CA2128942822

Gene: NFKBIA

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.35401591A= , CM000676.2:g.35401591A=	GRCh38
NC_000014.8:g.35870797A= , CM000676.1:g.35870797A=	GRCh37
NC_000014.7:g.34940548A=	NCBI36
NG_007571.1:g.8148T= , LRG_89:g.8148T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000553342.2:c.*422T=	ENSP00000451281.2:n.*422T=
ENST00000697954.1:n.1585T=
ENST00000697955.1:n.1624T=
ENST00000697956.1:n.1652T=
ENST00000697957.1:n.1771T=
ENST00000697958.1:n.2426T=
ENST00000697959.1:n.2104T=
ENST00000697960.1:n.2520T=
ENST00000697961.1:c.*791T=	ENSP00000513487.1:n.*791T=
ENST00000216797.10:c.*422T= MANE Select	ENSP00000216797.6:n.*422T=
ENST00000216797.9:c.*422T=	ENSP00000216797.5:n.*422T=
ENST00000554001.5:c.*1018T=	ENSP00000450537.1:n.*1018T=
ENST00000557140.5:c.*422T=	ENSP00000451257.1:n.*422T=
ENST00000557389.1:c.*422T=	ENSP00000450514.1:n.*422T=
NM_020529.2:c.*422T= , LRG_89t1:c.*422T=	NP_065390.1:n.*422T=
NM_020529.3:c.*422T= MANE Select	NP_065390.1:n.*422T=