Canonical Allele Identifier: CA705268263

Gene: NFKBIA

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.35402011G>C , CM000676.2:g.35402011G>C	GRCh38
NC_000014.8:g.35871217G>C , CM000676.1:g.35871217G>C	GRCh37
NC_000014.7:g.34940968G>C	NCBI36
NG_007571.1:g.7728C>G , LRG_89:g.7728C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000553342.2:c.*2C>G	ENSP00000451281.2:n.*2C>G
ENST00000557459.2:n.1784C>G
ENST00000697954.1:n.1165C>G
ENST00000697955.1:n.1204C>G
ENST00000697956.1:n.1232C>G
ENST00000697957.1:n.1351C>G
ENST00000697958.1:n.2006C>G
ENST00000697959.1:n.1684C>G
ENST00000697960.1:n.2100C>G
ENST00000697961.1:c.*371C>G	ENSP00000513487.1:n.*371C>G
ENST00000697962.1:c.*371C>G	ENSP00000513488.1:n.*371C>G
ENST00000697965.1:n.164C>G
ENST00000216797.10:c.*2C>G MANE Select	ENSP00000216797.6:n.*2C>G
ENST00000216797.9:c.*2C>G	ENSP00000216797.5:n.*2C>G
ENST00000554001.5:c.*598C>G	ENSP00000450537.1:n.*598C>G
ENST00000555371.1:n.605C>G
ENST00000557140.5:c.*2C>G	ENSP00000451257.1:n.*2C>G
ENST00000557389.1:c.*2C>G	ENSP00000450514.1:n.*2C>G
NM_020529.2:c.*2C>G , LRG_89t1:c.*2C>G	NP_065390.1:n.*2C>G
NM_020529.3:c.*2C>G MANE Select	NP_065390.1:n.*2C>G