Canonical Allele Identifier: CA7155548
Community Standard Title: NM_020529.3(NFKBIA):c.228-15C>T
Gene: NFKBIA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.35403813G>A , CM000676.2:g.35403813G>A GRCh38
NC_000014.8:g.35873019G>A , CM000676.1:g.35873019G>A GRCh37
NC_000014.7:g.34942770G>A NCBI36
NG_007571.1:g.5926C>T , LRG_89:g.5926C>T

Transcript Alleles

HGVS Amino-acid Change
NM_020529.3:c.228-15C>T MANE Select NP_065390.1:n.228-15C>T
ENST00000216797.10:c.228-15C>T MANE Select ENSP00000216797.6:n.228-15C>T
NM_020529.2:c.228-15C>T , LRG_89t1:c.228-15C>T NP_065390.1:n.228-15C>T
ENST00000216797.9:c.228-15C>T ENSP00000216797.5:n.228-15C>T
ENST00000553342.1:c.156-15C>T ENSP00000451281.1:n.156-15C>T
ENST00000553342.2:c.156-15C>T ENSP00000451281.2:n.156-15C>T
ENST00000554001.5:c.228-453C>T ENSP00000450537.1:n.228-453C>T
ENST00000555629.1:n.333-15C>T
ENST00000557100.5:n.284-15C>T
ENST00000557140.5:c.228-15C>T ENSP00000451257.1:n.228-15C>T
ENST00000557389.1:c.-58C>T ENSP00000450514.1:n.-58C>T
ENST00000557459.1:n.326-15C>T
ENST00000557459.2:n.326-15C>T
ENST00000697956.1:n.92C>T
ENST00000697957.1:n.333-15C>T
ENST00000697958.1:n.326-15C>T
ENST00000697959.1:n.333-15C>T
ENST00000697960.1:n.313-15C>T
ENST00000697961.1:c.228-15C>T ENSP00000513487.1:n.228-15C>T
ENST00000697966.1:n.246-15C>T