Canonical Allele Identifier: CA2624569269
Gene: NFKBIA HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.35404624dup , CM000676.2:g.35404624dup GRCh38
NC_000014.8:g.35873830dup , CM000676.1:g.35873830dup GRCh37
NC_000014.7:g.34943581dup NCBI36
NG_007571.1:g.5119dup , LRG_89:g.5119dup

Transcript Alleles

HGVS Amino-acid change
ENST00000553342.2:c.25dup ENSP00000451281.2:p.Gln9ProfsTer?
ENST00000557459.2:n.123dup
ENST00000697957.1:n.130dup
ENST00000697958.1:n.123dup
ENST00000697959.1:n.130dup
ENST00000697960.1:n.110dup
ENST00000697961.1:c.25dup ENSP00000513487.1:p.Gln9ProfsTer?
ENST00000697966.1:n.49-6dup
ENST00000216797.10:c.25dup MANE Select ENSP00000216797.6:p.Gln9ProfsTer?
ENST00000216797.9:c.25dup ENSP00000216797.5:p.Gln9ProfsTer?
ENST00000553342.1:c.25dup ENSP00000451281.1:p.Gln9ProfsTer?
ENST00000554001.5:c.25dup ENSP00000450537.1:p.Gln9ProfsTer?
ENST00000555629.1:n.130dup
ENST00000557100.5:n.81dup
ENST00000557140.5:c.25dup ENSP00000451257.1:p.Gln9ProfsTer?
ENST00000557459.1:n.123dup
NM_020529.2:c.25dup , LRG_89t1:c.25dup NP_065390.1:p.Gln9ProfsTer?
NM_020529.3:c.25dup MANE Select NP_065390.1:p.Gln9ProfsTer?