Canonical Allele Identifier: CA2729397789

Gene: NFKBIA

Linked Data

• dbSNP Id: rs2138829072

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.35401585C>T , CM000676.2:g.35401585C>T	GRCh38
NC_000014.8:g.35870791C>T , CM000676.1:g.35870791C>T	GRCh37
NC_000014.7:g.34940542C>T	NCBI36
NG_007571.1:g.8154G>A , LRG_89:g.8154G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000553342.2:c.*428G>A	ENSP00000451281.2:n.*428G>A
ENST00000697954.1:n.1591G>A
ENST00000697955.1:n.1630G>A
ENST00000697956.1:n.1658G>A
ENST00000697957.1:n.1777G>A
ENST00000697958.1:n.2432G>A
ENST00000697959.1:n.2110G>A
ENST00000697960.1:n.2526G>A
ENST00000697961.1:c.*797G>A	ENSP00000513487.1:n.*797G>A
ENST00000216797.10:c.*428G>A MANE Select	ENSP00000216797.6:n.*428G>A
ENST00000216797.9:c.*428G>A	ENSP00000216797.5:n.*428G>A
ENST00000554001.5:c.*1024G>A	ENSP00000450537.1:n.*1024G>A
ENST00000557140.5:c.*428G>A	ENSP00000451257.1:n.*428G>A
ENST00000557389.1:c.*428G>A	ENSP00000450514.1:n.*428G>A
NM_020529.2:c.*428G>A , LRG_89t1:c.*428G>A	NP_065390.1:n.*428G>A
NM_020529.3:c.*428G>A MANE Select	NP_065390.1:n.*428G>A