Canonical Allele Identifier: CA258861689

Gene: NFKBIA

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.35403165C>T , CM000676.2:g.35403165C>T	GRCh38
NC_000014.8:g.35872371C>T , CM000676.1:g.35872371C>T	GRCh37
NC_000014.7:g.34942122C>T	NCBI36
NG_007571.1:g.6574G>A , LRG_89:g.6574G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_020529.3:c.532G>A MANE Select	NP_065390.1:p.Ala178Thr
ENST00000216797.10:c.532G>A MANE Select	ENSP00000216797.6:p.Ala178Thr
NM_020529.2:c.532G>A , LRG_89t1:c.532G>A	NP_065390.1:p.Ala178Thr
ENST00000216797.9:c.532G>A	ENSP00000216797.5:p.Ala178Thr
ENST00000553342.2:c.460G>A	ENSP00000451281.2:p.Ala154Thr
ENST00000554001.5:c.*174G>A	ENSP00000450537.1:n.*174G>A
ENST00000555371.1:n.74G>A
ENST00000556664.1:n.266G>A
ENST00000557100.5:n.588G>A
ENST00000557140.5:c.532G>A	ENSP00000451257.1:p.Ala178Thr
ENST00000557389.1:c.262G>A	ENSP00000450514.1:p.Ala88Thr
ENST00000557459.1:n.630G>A
ENST00000557459.2:n.630G>A
ENST00000697954.1:n.344G>A
ENST00000697955.1:n.490G>A
ENST00000697956.1:n.411G>A
ENST00000697957.1:n.637G>A
ENST00000697958.1:n.959G>A
ENST00000697959.1:n.637G>A
ENST00000697960.1:n.946G>A
ENST00000697961.1:c.532G>A	ENSP00000513487.1:p.Ala178Thr
ENST00000697962.1:c.262G>A	ENSP00000513488.1:p.Ala88Thr
ENST00000697966.1:n.550G>A