Canonical Allele Identifier: CA258860922

Gene: NFKBIA

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.35402434T>C , CM000676.2:g.35402434T>C	GRCh38
NC_000014.8:g.35871640T>C , CM000676.1:g.35871640T>C	GRCh37
NC_000014.7:g.34941391T>C	NCBI36
NG_007571.1:g.7305A>G , LRG_89:g.7305A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_020529.3:c.866A>G MANE Select	NP_065390.1:p.Tyr289Cys
ENST00000216797.10:c.866A>G MANE Select	ENSP00000216797.6:p.Tyr289Cys
NM_020529.2:c.866A>G , LRG_89t1:c.866A>G	NP_065390.1:p.Tyr289Cys
ENST00000216797.9:c.866A>G	ENSP00000216797.5:p.Tyr289Cys
ENST00000553342.2:c.794A>G	ENSP00000451281.2:p.Tyr265Cys
ENST00000554001.5:c.*508A>G	ENSP00000450537.1:n.*508A>G
ENST00000555371.1:n.515A>G
ENST00000557140.5:c.737A>G	ENSP00000451257.1:p.Tyr246Cys
ENST00000557389.1:c.596A>G	ENSP00000450514.1:p.Tyr199Cys
ENST00000557459.2:n.1361A>G
ENST00000697954.1:n.1075A>G
ENST00000697955.1:n.1114A>G
ENST00000697956.1:n.1142A>G
ENST00000697957.1:n.1261A>G
ENST00000697958.1:n.1583A>G
ENST00000697959.1:n.1261A>G
ENST00000697960.1:n.1677A>G
ENST00000697961.1:c.866A>G	ENSP00000513487.1:p.Tyr289Cys
ENST00000697962.1:c.596A>G	ENSP00000513488.1:p.Tyr199Cys
ENST00000697965.1:n.70A>G
ENST00000697966.1:n.884A>G