Canonical Allele Identifier: CA2128942824

Gene: NFKBIA

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.35401592C= , CM000676.2:g.35401592C=	GRCh38
NC_000014.8:g.35870798C= , CM000676.1:g.35870798C=	GRCh37
NC_000014.7:g.34940549C=	NCBI36
NG_007571.1:g.8147G= , LRG_89:g.8147G=

Transcript Alleles

HGVS	Amino-acid Change
NM_020529.3:c.*421G= MANE Select	NP_065390.1:n.*421G=
ENST00000216797.10:c.*421G= MANE Select	ENSP00000216797.6:n.*421G=
NM_020529.2:c.*421G= , LRG_89t1:c.*421G=	NP_065390.1:n.*421G=
ENST00000216797.9:c.*421G=	ENSP00000216797.5:n.*421G=
ENST00000553342.2:c.*421G=	ENSP00000451281.2:n.*421G=
ENST00000554001.5:c.*1017G=	ENSP00000450537.1:n.*1017G=
ENST00000557140.5:c.*421G=	ENSP00000451257.1:n.*421G=
ENST00000557389.1:c.*421G=	ENSP00000450514.1:n.*421G=
ENST00000697954.1:n.1584G=
ENST00000697955.1:n.1623G=
ENST00000697956.1:n.1651G=
ENST00000697957.1:n.1770G=
ENST00000697958.1:n.2425G=
ENST00000697959.1:n.2103G=
ENST00000697960.1:n.2519G=
ENST00000697961.1:c.*790G=	ENSP00000513487.1:n.*790G=