Canonical Allele Identifier: CA2128944029

Gene: NFKBIA

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.35403720G= , CM000676.2:g.35403720G=	GRCh38
NC_000014.8:g.35872926G= , CM000676.1:g.35872926G=	GRCh37
NC_000014.7:g.34942677G=	NCBI36
NG_007571.1:g.6019C= , LRG_89:g.6019C=

Transcript Alleles

HGVS	Amino-acid Change
NM_020529.3:c.306C= MANE Select	NP_065390.1:p.Ala102=
ENST00000216797.10:c.306C= MANE Select	ENSP00000216797.6:p.Ala102=
NM_020529.2:c.306C= , LRG_89t1:c.306C=	NP_065390.1:p.Ala102=
ENST00000216797.9:c.306C=	ENSP00000216797.5:p.Ala102=
ENST00000553342.2:c.234C=	ENSP00000451281.2:p.Ala78=
ENST00000554001.5:c.228-360C=	ENSP00000450537.1:n.228-360C=
ENST00000555629.1:n.411C=
ENST00000557100.5:n.362C=
ENST00000557140.5:c.306C=	ENSP00000451257.1:p.Ala102=
ENST00000557389.1:c.36C=	ENSP00000450514.1:p.Ala12=
ENST00000557459.1:n.404C=
ENST00000557459.2:n.404C=
ENST00000697956.1:n.185C=
ENST00000697957.1:n.411C=
ENST00000697958.1:n.404C=
ENST00000697959.1:n.411C=
ENST00000697960.1:n.391C=
ENST00000697961.1:c.306C=	ENSP00000513487.1:p.Ala102=
ENST00000697962.1:c.36C=	ENSP00000513488.1:p.Ala12=
ENST00000697966.1:n.324C=