Canonical Allele Identifier: CA2128944705
Gene: NFKBIA HGNC NCBI

Linked Data

dbSNP Id: rs2052772000

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.35404673_35404702del , CM000676.2:g.35404673_35404702del GRCh38
NC_000014.8:g.35873879_35873908del , CM000676.1:g.35873879_35873908del GRCh37
NC_000014.7:g.34943630_34943659del NCBI36
NG_007571.1:g.5042_5071del , LRG_89:g.5042_5071del

Transcript Alleles

HGVS Amino-acid Change
ENST00000553342.2:c.-53_-24del ENSP00000451281.2:n.-53_-24del
ENST00000557459.2:n.46_75del
ENST00000697957.1:n.53_82del
ENST00000697958.1:n.46_75del
ENST00000697959.1:n.53_82del
ENST00000697960.1:n.33_62del
ENST00000697961.1:c.-53_-24del ENSP00000513487.1:n.-53_-24del
ENST00000216797.10:c.-53_-24del MANE Select ENSP00000216797.6:n.-53_-24del
ENST00000216797.9:c.-53_-24del ENSP00000216797.5:n.-53_-24del
ENST00000554001.5:c.-53_-24del ENSP00000450537.1:n.-53_-24del
ENST00000555629.1:n.53_82del
ENST00000557140.5:c.-53_-24del ENSP00000451257.1:n.-53_-24del
ENST00000557459.1:n.46_75del
NM_020529.2:c.-53_-24del , LRG_89t1:c.-53_-24del NP_065390.1:n.-53_-24del
NM_020529.3:c.-53_-24del MANE Select NP_065390.1:n.-53_-24del