Canonical Allele Identifier: CA2624566878

Gene: NFKBIA

Linked Data

• gnomAD v4: 14-35401690-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.35401690G>T , CM000676.2:g.35401690G>T	GRCh38
NC_000014.8:g.35870896G>T , CM000676.1:g.35870896G>T	GRCh37
NC_000014.7:g.34940647G>T	NCBI36
NG_007571.1:g.8049C>A , LRG_89:g.8049C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000553342.2:c.*323C>A	ENSP00000451281.2:n.*323C>A
ENST00000697954.1:n.1486C>A
ENST00000697955.1:n.1525C>A
ENST00000697956.1:n.1553C>A
ENST00000697957.1:n.1672C>A
ENST00000697958.1:n.2327C>A
ENST00000697959.1:n.2005C>A
ENST00000697960.1:n.2421C>A
ENST00000697961.1:c.*692C>A	ENSP00000513487.1:n.*692C>A
ENST00000216797.10:c.*323C>A MANE Select	ENSP00000216797.6:n.*323C>A
ENST00000216797.9:c.*323C>A	ENSP00000216797.5:n.*323C>A
ENST00000554001.5:c.*919C>A	ENSP00000450537.1:n.*919C>A
ENST00000557140.5:c.*323C>A	ENSP00000451257.1:n.*323C>A
ENST00000557389.1:c.*323C>A	ENSP00000450514.1:n.*323C>A
NM_020529.2:c.*323C>A , LRG_89t1:c.*323C>A	NP_065390.1:n.*323C>A
NM_020529.3:c.*323C>A MANE Select	NP_065390.1:n.*323C>A