Canonical Allele Identifier: CA7155539

Gene: NFKBIA

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.35403783G>A , CM000676.2:g.35403783G>A	GRCh38
NC_000014.8:g.35872989G>A , CM000676.1:g.35872989G>A	GRCh37
NC_000014.7:g.34942740G>A	NCBI36
NG_007571.1:g.5956C>T , LRG_89:g.5956C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000553342.2:c.171C>T	ENSP00000451281.2:p.Ala57=
ENST00000557459.2:n.341C>T
ENST00000697956.1:n.122C>T
ENST00000697957.1:n.348C>T
ENST00000697958.1:n.341C>T
ENST00000697959.1:n.348C>T
ENST00000697960.1:n.328C>T
ENST00000697961.1:c.243C>T	ENSP00000513487.1:p.Ala81=
ENST00000697966.1:n.261C>T
ENST00000216797.10:c.243C>T MANE Select	ENSP00000216797.6:p.Ala81=
ENST00000216797.9:c.243C>T	ENSP00000216797.5:p.Ala81=
ENST00000553342.1:c.171C>T	ENSP00000451281.1:p.Ala57=
ENST00000554001.5:c.228-423C>T	ENSP00000450537.1:n.228-423C>T
ENST00000555629.1:n.348C>T
ENST00000557100.5:n.299C>T
ENST00000557140.5:c.243C>T	ENSP00000451257.1:p.Ala81=
ENST00000557389.1:c.-28C>T	ENSP00000450514.1:n.-28C>T
ENST00000557459.1:n.341C>T
NM_020529.2:c.243C>T , LRG_89t1:c.243C>T	NP_065390.1:p.Ala81=
NM_020529.3:c.243C>T MANE Select	NP_065390.1:p.Ala81=