Canonical Allele Identifier: CA389453503

Gene: NFKBIA

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.35403294A>C , CM000676.2:g.35403294A>C	GRCh38
NC_000014.8:g.35872500A>C , CM000676.1:g.35872500A>C	GRCh37
NC_000014.7:g.34942251A>C	NCBI36
NG_007571.1:g.6445T>G , LRG_89:g.6445T>G

Transcript Alleles

HGVS	Amino-acid Change
NM_020529.3:c.403T>G MANE Select	NP_065390.1:p.Cys135Gly
ENST00000216797.10:c.403T>G MANE Select	ENSP00000216797.6:p.Cys135Gly
NM_020529.2:c.403T>G , LRG_89t1:c.403T>G	NP_065390.1:p.Cys135Gly
ENST00000216797.9:c.403T>G	ENSP00000216797.5:p.Cys135Gly
ENST00000553342.2:c.331T>G	ENSP00000451281.2:p.Cys111Gly
ENST00000554001.5:c.*45T>G	ENSP00000450537.1:n.*45T>G
ENST00000556664.1:n.137T>G
ENST00000557100.5:n.459T>G
ENST00000557140.5:c.403T>G	ENSP00000451257.1:p.Cys135Gly
ENST00000557389.1:c.133T>G	ENSP00000450514.1:p.Cys45Gly
ENST00000557459.1:n.501T>G
ENST00000557459.2:n.501T>G
ENST00000697954.1:n.215T>G
ENST00000697955.1:n.361T>G
ENST00000697956.1:n.282T>G
ENST00000697957.1:n.508T>G
ENST00000697958.1:n.830T>G
ENST00000697959.1:n.508T>G
ENST00000697960.1:n.817T>G
ENST00000697961.1:c.403T>G	ENSP00000513487.1:p.Cys135Gly
ENST00000697962.1:c.133T>G	ENSP00000513488.1:p.Cys45Gly
ENST00000697966.1:n.421T>G