Canonical Allele Identifier: CA2128942836

Gene: NFKBIA

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.35401619T= , CM000676.2:g.35401619T=	GRCh38
NC_000014.8:g.35870825T= , CM000676.1:g.35870825T=	GRCh37
NC_000014.7:g.34940576T=	NCBI36
NG_007571.1:g.8120A= , LRG_89:g.8120A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000553342.2:c.*394A=	ENSP00000451281.2:n.*394A=
ENST00000697954.1:n.1557A=
ENST00000697955.1:n.1596A=
ENST00000697956.1:n.1624A=
ENST00000697957.1:n.1743A=
ENST00000697958.1:n.2398A=
ENST00000697959.1:n.2076A=
ENST00000697960.1:n.2492A=
ENST00000697961.1:c.*763A=	ENSP00000513487.1:n.*763A=
ENST00000216797.10:c.*394A= MANE Select	ENSP00000216797.6:n.*394A=
ENST00000216797.9:c.*394A=	ENSP00000216797.5:n.*394A=
ENST00000554001.5:c.*990A=	ENSP00000450537.1:n.*990A=
ENST00000557140.5:c.*394A=	ENSP00000451257.1:n.*394A=
ENST00000557389.1:c.*394A=	ENSP00000450514.1:n.*394A=
NM_020529.2:c.*394A= , LRG_89t1:c.*394A=	NP_065390.1:n.*394A=
NM_020529.3:c.*394A= MANE Select	NP_065390.1:n.*394A=