Canonical Allele Identifier: CA2996383201

Gene: NFKBIA

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.35404613dup , CM000676.2:g.35404613dup	GRCh38
NC_000014.8:g.35873819dup , CM000676.1:g.35873819dup	GRCh37
NC_000014.7:g.34943570dup	NCBI36
NG_007571.1:g.5128dup , LRG_89:g.5128dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000553342.2:c.34dup	ENSP00000451281.2:p.Ala12GlyfsTer?
ENST00000557459.2:n.132dup
ENST00000697957.1:n.139dup
ENST00000697958.1:n.132dup
ENST00000697959.1:n.139dup
ENST00000697960.1:n.119dup
ENST00000697961.1:c.34dup	ENSP00000513487.1:p.Ala12GlyfsTer?
ENST00000697966.1:n.52dup
ENST00000216797.10:c.34dup MANE Select	ENSP00000216797.6:p.Ala12GlyfsTer?
ENST00000216797.9:c.34dup	ENSP00000216797.5:p.Ala12GlyfsTer?
ENST00000553342.1:c.34dup	ENSP00000451281.1:p.Ala12GlyfsTer?
ENST00000554001.5:c.34dup	ENSP00000450537.1:p.Ala12GlyfsTer?
ENST00000555629.1:n.139dup
ENST00000557100.5:n.90dup
ENST00000557140.5:c.34dup	ENSP00000451257.1:p.Ala12GlyfsTer?
ENST00000557459.1:n.132dup
NM_020529.2:c.34dup , LRG_89t1:c.34dup	NP_065390.1:p.Ala12GlyfsTer?
NM_020529.3:c.34dup MANE Select	NP_065390.1:p.Ala12GlyfsTer?