Canonical Allele Identifier: CA389455372
Gene: NFKBIA HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.35404572G>C , CM000676.2:g.35404572G>C GRCh38
NC_000014.8:g.35873778G>C , CM000676.1:g.35873778G>C GRCh37
NC_000014.7:g.34943529G>C NCBI36
NG_007571.1:g.5167C>G , LRG_89:g.5167C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000553342.2:c.73C>G ENSP00000451281.2:p.Leu25Val
ENST00000557459.2:n.171C>G
ENST00000697957.1:n.178C>G
ENST00000697958.1:n.171C>G
ENST00000697959.1:n.178C>G
ENST00000697960.1:n.158C>G
ENST00000697961.1:c.73C>G ENSP00000513487.1:p.Leu25Val
ENST00000697966.1:n.91C>G
ENST00000216797.10:c.73C>G MANE Select ENSP00000216797.6:p.Leu25Val
ENST00000216797.9:c.73C>G ENSP00000216797.5:p.Leu25Val
ENST00000553342.1:c.73C>G ENSP00000451281.1:p.Leu25Val
ENST00000554001.5:c.73C>G ENSP00000450537.1:p.Leu25Val
ENST00000555629.1:n.178C>G
ENST00000557100.5:n.129C>G
ENST00000557140.5:c.73C>G ENSP00000451257.1:p.Leu25Val
ENST00000557459.1:n.171C>G
NM_020529.2:c.73C>G , LRG_89t1:c.73C>G NP_065390.1:p.Leu25Val
NM_020529.3:c.73C>G MANE Select NP_065390.1:p.Leu25Val