Canonical Allele Identifier: CA2128944664

Gene: NFKBIA

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.35404619T= , CM000676.2:g.35404619T=	GRCh38
NC_000014.8:g.35873825T= , CM000676.1:g.35873825T=	GRCh37
NC_000014.7:g.34943576T=	NCBI36
NG_007571.1:g.5120A= , LRG_89:g.5120A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000553342.2:c.26A=	ENSP00000451281.2:p.Gln9=
ENST00000557459.2:n.124A=
ENST00000697957.1:n.131A=
ENST00000697958.1:n.124A=
ENST00000697959.1:n.131A=
ENST00000697960.1:n.111A=
ENST00000697961.1:c.26A=	ENSP00000513487.1:p.Gln9=
ENST00000697966.1:n.49-5A=
ENST00000216797.10:c.26A= MANE Select	ENSP00000216797.6:p.Gln9=
ENST00000216797.9:c.26A=	ENSP00000216797.5:p.Gln9=
ENST00000553342.1:c.26A=	ENSP00000451281.1:p.Gln9=
ENST00000554001.5:c.26A=	ENSP00000450537.1:p.Gln9=
ENST00000555629.1:n.131A=
ENST00000557100.5:n.82A=
ENST00000557140.5:c.26A=	ENSP00000451257.1:p.Gln9=
ENST00000557459.1:n.124A=
NM_020529.2:c.26A= , LRG_89t1:c.26A=	NP_065390.1:p.Gln9=
NM_020529.3:c.26A= MANE Select	NP_065390.1:p.Gln9=