Canonical Allele Identifier: CA2624566884

Gene: NFKBIA

Linked Data

• gnomAD v4: 14-35401700-T-G

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.35401700T>G , CM000676.2:g.35401700T>G	GRCh38
NC_000014.8:g.35870906T>G , CM000676.1:g.35870906T>G	GRCh37
NC_000014.7:g.34940657T>G	NCBI36
NG_007571.1:g.8039A>C , LRG_89:g.8039A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000553342.2:c.*313A>C	ENSP00000451281.2:n.*313A>C
ENST00000697954.1:n.1476A>C
ENST00000697955.1:n.1515A>C
ENST00000697956.1:n.1543A>C
ENST00000697957.1:n.1662A>C
ENST00000697958.1:n.2317A>C
ENST00000697959.1:n.1995A>C
ENST00000697960.1:n.2411A>C
ENST00000697961.1:c.*682A>C	ENSP00000513487.1:n.*682A>C
ENST00000216797.10:c.*313A>C MANE Select	ENSP00000216797.6:n.*313A>C
ENST00000216797.9:c.*313A>C	ENSP00000216797.5:n.*313A>C
ENST00000554001.5:c.*909A>C	ENSP00000450537.1:n.*909A>C
ENST00000557140.5:c.*313A>C	ENSP00000451257.1:n.*313A>C
ENST00000557389.1:c.*313A>C	ENSP00000450514.1:n.*313A>C
NM_020529.2:c.*313A>C , LRG_89t1:c.*313A>C	NP_065390.1:n.*313A>C
NM_020529.3:c.*313A>C MANE Select	NP_065390.1:n.*313A>C