Canonical Allele Identifier: CA2624566830

Gene: NFKBIA

Linked Data

• gnomAD v4: 14-35401602-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.35401602A>G , CM000676.2:g.35401602A>G	GRCh38
NC_000014.8:g.35870808A>G , CM000676.1:g.35870808A>G	GRCh37
NC_000014.7:g.34940559A>G	NCBI36
NG_007571.1:g.8137T>C , LRG_89:g.8137T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000553342.2:c.*411T>C	ENSP00000451281.2:n.*411T>C
ENST00000697954.1:n.1574T>C
ENST00000697955.1:n.1613T>C
ENST00000697956.1:n.1641T>C
ENST00000697957.1:n.1760T>C
ENST00000697958.1:n.2415T>C
ENST00000697959.1:n.2093T>C
ENST00000697960.1:n.2509T>C
ENST00000697961.1:c.*780T>C	ENSP00000513487.1:n.*780T>C
ENST00000216797.10:c.*411T>C MANE Select	ENSP00000216797.6:n.*411T>C
ENST00000216797.9:c.*411T>C	ENSP00000216797.5:n.*411T>C
ENST00000554001.5:c.*1007T>C	ENSP00000450537.1:n.*1007T>C
ENST00000557140.5:c.*411T>C	ENSP00000451257.1:n.*411T>C
ENST00000557389.1:c.*411T>C	ENSP00000450514.1:n.*411T>C
NM_020529.2:c.*411T>C , LRG_89t1:c.*411T>C	NP_065390.1:n.*411T>C
NM_020529.3:c.*411T>C MANE Select	NP_065390.1:n.*411T>C