Canonical Allele Identifier: CA2128944659

Gene: NFKBIA

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.35404609G= , CM000676.2:g.35404609G=	GRCh38
NC_000014.8:g.35873815G= , CM000676.1:g.35873815G=	GRCh37
NC_000014.7:g.34943566G=	NCBI36
NG_007571.1:g.5130C= , LRG_89:g.5130C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000553342.2:c.36C=	ENSP00000451281.2:p.Ala12=
ENST00000557459.2:n.134C=
ENST00000697957.1:n.141C=
ENST00000697958.1:n.134C=
ENST00000697959.1:n.141C=
ENST00000697960.1:n.121C=
ENST00000697961.1:c.36C=	ENSP00000513487.1:p.Ala12=
ENST00000697966.1:n.54C=
ENST00000216797.10:c.36C= MANE Select	ENSP00000216797.6:p.Ala12=
ENST00000216797.9:c.36C=	ENSP00000216797.5:p.Ala12=
ENST00000553342.1:c.36C=	ENSP00000451281.1:p.Ala12=
ENST00000554001.5:c.36C=	ENSP00000450537.1:p.Ala12=
ENST00000555629.1:n.141C=
ENST00000557100.5:n.92C=
ENST00000557140.5:c.36C=	ENSP00000451257.1:p.Ala12=
ENST00000557459.1:n.134C=
NM_020529.2:c.36C= , LRG_89t1:c.36C=	NP_065390.1:p.Ala12=
NM_020529.3:c.36C= MANE Select	NP_065390.1:p.Ala12=