Canonical Allele Identifier: CA2624566838

Gene: NFKBIA

Linked Data

• gnomAD v4: 14-35401624-A-C

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.35401624A>C , CM000676.2:g.35401624A>C	GRCh38
NC_000014.8:g.35870830A>C , CM000676.1:g.35870830A>C	GRCh37
NC_000014.7:g.34940581A>C	NCBI36
NG_007571.1:g.8115T>G , LRG_89:g.8115T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000553342.2:c.*389T>G	ENSP00000451281.2:n.*389T>G
ENST00000697954.1:n.1552T>G
ENST00000697955.1:n.1591T>G
ENST00000697956.1:n.1619T>G
ENST00000697957.1:n.1738T>G
ENST00000697958.1:n.2393T>G
ENST00000697959.1:n.2071T>G
ENST00000697960.1:n.2487T>G
ENST00000697961.1:c.*758T>G	ENSP00000513487.1:n.*758T>G
ENST00000216797.10:c.*389T>G MANE Select	ENSP00000216797.6:n.*389T>G
ENST00000216797.9:c.*389T>G	ENSP00000216797.5:n.*389T>G
ENST00000554001.5:c.*985T>G	ENSP00000450537.1:n.*985T>G
ENST00000557140.5:c.*389T>G	ENSP00000451257.1:n.*389T>G
ENST00000557389.1:c.*389T>G	ENSP00000450514.1:n.*389T>G
NM_020529.2:c.*389T>G , LRG_89t1:c.*389T>G	NP_065390.1:n.*389T>G
NM_020529.3:c.*389T>G MANE Select	NP_065390.1:n.*389T>G