Canonical Allele Identifier: CA7155490

Gene: NFKBIA

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.35403380C>T , CM000676.2:g.35403380C>T	GRCh38
NC_000014.8:g.35872586C>T , CM000676.1:g.35872586C>T	GRCh37
NC_000014.7:g.34942337C>T	NCBI36
NG_007571.1:g.6359G>A , LRG_89:g.6359G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_020529.3:c.337-20G>A MANE Select	NP_065390.1:n.337-20G>A
ENST00000216797.10:c.337-20G>A MANE Select	ENSP00000216797.6:n.337-20G>A
NM_020529.2:c.337-20G>A , LRG_89t1:c.337-20G>A	NP_065390.1:n.337-20G>A
ENST00000216797.9:c.337-20G>A	ENSP00000216797.5:n.337-20G>A
ENST00000553342.2:c.265-20G>A	ENSP00000451281.2:n.265-20G>A
ENST00000554001.5:c.228-20G>A	ENSP00000450537.1:n.228-20G>A
ENST00000556664.1:n.51G>A
ENST00000557100.5:n.393-20G>A
ENST00000557140.5:c.337-20G>A	ENSP00000451257.1:n.337-20G>A
ENST00000557389.1:c.67-20G>A	ENSP00000450514.1:n.67-20G>A
ENST00000557459.1:n.435-20G>A
ENST00000557459.2:n.435-20G>A
ENST00000697954.1:n.129G>A
ENST00000697955.1:n.275G>A
ENST00000697956.1:n.216-20G>A
ENST00000697957.1:n.442-20G>A
ENST00000697958.1:n.744G>A
ENST00000697959.1:n.442-20G>A
ENST00000697960.1:n.731G>A
ENST00000697961.1:c.337-20G>A	ENSP00000513487.1:n.337-20G>A
ENST00000697962.1:c.67-20G>A	ENSP00000513488.1:n.67-20G>A
ENST00000697966.1:n.355-20G>A