Canonical Allele Identifier: CA2128942859

Gene: NFKBIA

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.35401670A= , CM000676.2:g.35401670A=	GRCh38
NC_000014.8:g.35870876A= , CM000676.1:g.35870876A=	GRCh37
NC_000014.7:g.34940627A=	NCBI36
NG_007571.1:g.8069T= , LRG_89:g.8069T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000553342.2:c.*343T=	ENSP00000451281.2:n.*343T=
ENST00000697954.1:n.1506T=
ENST00000697955.1:n.1545T=
ENST00000697956.1:n.1573T=
ENST00000697957.1:n.1692T=
ENST00000697958.1:n.2347T=
ENST00000697959.1:n.2025T=
ENST00000697960.1:n.2441T=
ENST00000697961.1:c.*712T=	ENSP00000513487.1:n.*712T=
ENST00000216797.10:c.*343T= MANE Select	ENSP00000216797.6:n.*343T=
ENST00000216797.9:c.*343T=	ENSP00000216797.5:n.*343T=
ENST00000554001.5:c.*939T=	ENSP00000450537.1:n.*939T=
ENST00000557140.5:c.*343T=	ENSP00000451257.1:n.*343T=
ENST00000557389.1:c.*343T=	ENSP00000450514.1:n.*343T=
NM_020529.2:c.*343T= , LRG_89t1:c.*343T=	NP_065390.1:n.*343T=
NM_020529.3:c.*343T= MANE Select	NP_065390.1:n.*343T=