Canonical Allele Identifier: CA389455249

Gene: NFKBIA

Linked Data - Variant Effect Evidence

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.35404518C>A , CM000676.2:g.35404518C>A	GRCh38
NC_000014.8:g.35873724C>A , CM000676.1:g.35873724C>A	GRCh37
NC_000014.7:g.34943475C>A	NCBI36
NG_007571.1:g.5221G>T , LRG_89:g.5221G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000553342.2:c.127G>T	ENSP00000451281.2:p.Glu43Ter
ENST00000557459.2:n.225G>T
ENST00000697957.1:n.232G>T
ENST00000697958.1:n.225G>T
ENST00000697959.1:n.232G>T
ENST00000697960.1:n.212G>T
ENST00000697961.1:c.127G>T	ENSP00000513487.1:p.Glu43Ter
ENST00000697966.1:n.145G>T
ENST00000216797.10:c.127G>T MANE Select	ENSP00000216797.6:p.Glu43Ter
ENST00000216797.9:c.127G>T	ENSP00000216797.5:p.Glu43Ter
ENST00000553342.1:c.127G>T	ENSP00000451281.1:p.Glu43Ter
ENST00000554001.5:c.127G>T	ENSP00000450537.1:p.Glu43Ter
ENST00000555629.1:n.232G>T
ENST00000557100.5:n.183G>T
ENST00000557140.5:c.127G>T	ENSP00000451257.1:p.Glu43Ter
ENST00000557459.1:n.225G>T
NM_020529.2:c.127G>T , LRG_89t1:c.127G>T	NP_065390.1:p.Glu43Ter
NM_020529.3:c.127G>T MANE Select	NP_065390.1:p.Glu43Ter