Canonical Allele Identifier: CA2128944748

Gene: NFKBIA

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.35404713G= , CM000676.2:g.35404713G=	GRCh38
NC_000014.8:g.35873919G= , CM000676.1:g.35873919G=	GRCh37
NC_000014.7:g.34943670G=	NCBI36
NG_007571.1:g.5026C= , LRG_89:g.5026C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000553342.2:c.-69C=	ENSP00000451281.2:n.-69C=
ENST00000557459.2:n.30C=
ENST00000697957.1:n.37C=
ENST00000697958.1:n.30C=
ENST00000697959.1:n.37C=
ENST00000697960.1:n.17C=
ENST00000697961.1:c.-69C=	ENSP00000513487.1:n.-69C=
ENST00000216797.10:c.-69C= MANE Select	ENSP00000216797.6:n.-69C=
ENST00000216797.9:c.-69C=	ENSP00000216797.5:n.-69C=
ENST00000554001.5:c.-69C=	ENSP00000450537.1:n.-69C=
ENST00000555629.1:n.37C=
ENST00000557140.5:c.-69C=	ENSP00000451257.1:n.-69C=
ENST00000557459.1:n.30C=
NM_020529.2:c.-69C= , LRG_89t1:c.-69C=	NP_065390.1:n.-69C=
NM_020529.3:c.-69C= MANE Select	NP_065390.1:n.-69C=