Canonical Allele Identifier: CA3038935604
Gene: NFKBIA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.35404533del , CM000676.2:g.35404533del GRCh38
NC_000014.8:g.35873739del , CM000676.1:g.35873739del GRCh37
NC_000014.7:g.34943490del NCBI36
NG_007571.1:g.5208del , LRG_89:g.5208del

Transcript Alleles

HGVS Amino-acid Change
ENST00000553342.2:c.114del ENSP00000451281.2:p.Asp39ThrfsTer27
ENST00000557459.2:n.212del
ENST00000697957.1:n.219del
ENST00000697958.1:n.212del
ENST00000697959.1:n.219del
ENST00000697960.1:n.199del
ENST00000697961.1:c.114del ENSP00000513487.1:p.Asp39ThrfsTer?
ENST00000697966.1:n.132del
ENST00000216797.10:c.114del MANE Select ENSP00000216797.6:p.Asp39ThrfsTer?
ENST00000216797.9:c.114del ENSP00000216797.5:p.Asp39ThrfsTer?
ENST00000553342.1:c.114del ENSP00000451281.1:p.Asp39ThrfsTer27
ENST00000554001.5:c.114del ENSP00000450537.1:p.Asp39ThrfsTer?
ENST00000555629.1:n.219del
ENST00000557100.5:n.170del
ENST00000557140.5:c.114del ENSP00000451257.1:p.Asp39ThrfsTer?
ENST00000557459.1:n.212del
NM_020529.2:c.114del , LRG_89t1:c.114del NP_065390.1:p.Asp39ThrfsTer?
NM_020529.3:c.114del MANE Select NP_065390.1:p.Asp39ThrfsTer?