Canonical Allele Identifier: CA2624566827

Gene: NFKBIA

Linked Data

• gnomAD v4: 14-35401594-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.35401594G>T , CM000676.2:g.35401594G>T	GRCh38
NC_000014.8:g.35870800G>T , CM000676.1:g.35870800G>T	GRCh37
NC_000014.7:g.34940551G>T	NCBI36
NG_007571.1:g.8145C>A , LRG_89:g.8145C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000553342.2:c.*419C>A	ENSP00000451281.2:n.*419C>A
ENST00000697954.1:n.1582C>A
ENST00000697955.1:n.1621C>A
ENST00000697956.1:n.1649C>A
ENST00000697957.1:n.1768C>A
ENST00000697958.1:n.2423C>A
ENST00000697959.1:n.2101C>A
ENST00000697960.1:n.2517C>A
ENST00000697961.1:c.*788C>A	ENSP00000513487.1:n.*788C>A
ENST00000216797.10:c.*419C>A MANE Select	ENSP00000216797.6:n.*419C>A
ENST00000216797.9:c.*419C>A	ENSP00000216797.5:n.*419C>A
ENST00000554001.5:c.*1015C>A	ENSP00000450537.1:n.*1015C>A
ENST00000557140.5:c.*419C>A	ENSP00000451257.1:n.*419C>A
ENST00000557389.1:c.*419C>A	ENSP00000450514.1:n.*419C>A
NM_020529.2:c.*419C>A , LRG_89t1:c.*419C>A	NP_065390.1:n.*419C>A
NM_020529.3:c.*419C>A MANE Select	NP_065390.1:n.*419C>A