Canonical Allele Identifier: CA7155480

Gene: NFKBIA

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.35403329T>C , CM000676.2:g.35403329T>C	GRCh38
NC_000014.8:g.35872535T>C , CM000676.1:g.35872535T>C	GRCh37
NC_000014.7:g.34942286T>C	NCBI36
NG_007571.1:g.6410A>G , LRG_89:g.6410A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_020529.3:c.368A>G MANE Select	NP_065390.1:p.Gln123Arg
ENST00000216797.10:c.368A>G MANE Select	ENSP00000216797.6:p.Gln123Arg
NM_020529.2:c.368A>G , LRG_89t1:c.368A>G	NP_065390.1:p.Gln123Arg
ENST00000216797.9:c.368A>G	ENSP00000216797.5:p.Gln123Arg
ENST00000553342.2:c.296A>G	ENSP00000451281.2:p.Gln99Arg
ENST00000554001.5:c.*10A>G	ENSP00000450537.1:n.*10A>G
ENST00000556664.1:n.102A>G
ENST00000557100.5:n.424A>G
ENST00000557140.5:c.368A>G	ENSP00000451257.1:p.Gln123Arg
ENST00000557389.1:c.98A>G	ENSP00000450514.1:p.Gln33Arg
ENST00000557459.1:n.466A>G
ENST00000557459.2:n.466A>G
ENST00000697954.1:n.180A>G
ENST00000697955.1:n.326A>G
ENST00000697956.1:n.247A>G
ENST00000697957.1:n.473A>G
ENST00000697958.1:n.795A>G
ENST00000697959.1:n.473A>G
ENST00000697960.1:n.782A>G
ENST00000697961.1:c.368A>G	ENSP00000513487.1:p.Gln123Arg
ENST00000697962.1:c.98A>G	ENSP00000513488.1:p.Gln33Arg
ENST00000697966.1:n.386A>G