Canonical Allele Identifier: CA2128942845

Gene: NFKBIA

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.35401637C= , CM000676.2:g.35401637C=	GRCh38
NC_000014.8:g.35870843C= , CM000676.1:g.35870843C=	GRCh37
NC_000014.7:g.34940594C=	NCBI36
NG_007571.1:g.8102G= , LRG_89:g.8102G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000553342.2:c.*376G=	ENSP00000451281.2:n.*376G=
ENST00000697954.1:n.1539G=
ENST00000697955.1:n.1578G=
ENST00000697956.1:n.1606G=
ENST00000697957.1:n.1725G=
ENST00000697958.1:n.2380G=
ENST00000697959.1:n.2058G=
ENST00000697960.1:n.2474G=
ENST00000697961.1:c.*745G=	ENSP00000513487.1:n.*745G=
ENST00000216797.10:c.*376G= MANE Select	ENSP00000216797.6:n.*376G=
ENST00000216797.9:c.*376G=	ENSP00000216797.5:n.*376G=
ENST00000554001.5:c.*972G=	ENSP00000450537.1:n.*972G=
ENST00000557140.5:c.*376G=	ENSP00000451257.1:n.*376G=
ENST00000557389.1:c.*376G=	ENSP00000450514.1:n.*376G=
NM_020529.2:c.*376G= , LRG_89t1:c.*376G=	NP_065390.1:n.*376G=
NM_020529.3:c.*376G= MANE Select	NP_065390.1:n.*376G=