Canonical Allele Identifier: CA10645265

Gene: NFKBIA

Linked Data - Expert Curation

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.35401887C>T , CM000676.2:g.35401887C>T	GRCh38
NC_000014.8:g.35871093C>T , CM000676.1:g.35871093C>T	GRCh37
NC_000014.7:g.34940844C>T	NCBI36
NG_007571.1:g.7852G>A , LRG_89:g.7852G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000553342.2:c.*126G>A	ENSP00000451281.2:n.*126G>A
ENST00000557459.2:n.1908G>A
ENST00000697954.1:n.1289G>A
ENST00000697955.1:n.1328G>A
ENST00000697956.1:n.1356G>A
ENST00000697957.1:n.1475G>A
ENST00000697958.1:n.2130G>A
ENST00000697959.1:n.1808G>A
ENST00000697960.1:n.2224G>A
ENST00000697961.1:c.*495G>A	ENSP00000513487.1:n.*495G>A
ENST00000216797.10:c.*126G>A MANE Select	ENSP00000216797.6:n.*126G>A
ENST00000216797.9:c.*126G>A	ENSP00000216797.5:n.*126G>A
ENST00000554001.5:c.*722G>A	ENSP00000450537.1:n.*722G>A
ENST00000557140.5:c.*126G>A	ENSP00000451257.1:n.*126G>A
ENST00000557389.1:c.*126G>A	ENSP00000450514.1:n.*126G>A
NM_020529.2:c.*126G>A , LRG_89t1:c.*126G>A	NP_065390.1:n.*126G>A
NM_020529.3:c.*126G>A MANE Select	NP_065390.1:n.*126G>A