Canonical Allele Identifier: CA2624566820

Gene: NFKBIA

Linked Data

• gnomAD v4: 14-35401583-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.35401583C>A , CM000676.2:g.35401583C>A	GRCh38
NC_000014.8:g.35870789C>A , CM000676.1:g.35870789C>A	GRCh37
NC_000014.7:g.34940540C>A	NCBI36
NG_007571.1:g.8156G>T , LRG_89:g.8156G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000553342.2:c.*430G>T	ENSP00000451281.2:n.*430G>T
ENST00000697954.1:n.1593G>T
ENST00000697955.1:n.1632G>T
ENST00000697956.1:n.1660G>T
ENST00000697957.1:n.1779G>T
ENST00000697958.1:n.2434G>T
ENST00000697959.1:n.2112G>T
ENST00000697960.1:n.2528G>T
ENST00000697961.1:c.*799G>T	ENSP00000513487.1:n.*799G>T
ENST00000216797.10:c.*430G>T MANE Select	ENSP00000216797.6:n.*430G>T
ENST00000216797.9:c.*430G>T	ENSP00000216797.5:n.*430G>T
ENST00000554001.5:c.*1026G>T	ENSP00000450537.1:n.*1026G>T
ENST00000557140.5:c.*430G>T	ENSP00000451257.1:n.*430G>T
ENST00000557389.1:c.*430G>T	ENSP00000450514.1:n.*430G>T
NM_020529.2:c.*430G>T , LRG_89t1:c.*430G>T	NP_065390.1:n.*430G>T
NM_020529.3:c.*430G>T MANE Select	NP_065390.1:n.*430G>T