Canonical Allele Identifier: CA389455488

Gene: NFKBIA

Linked Data

• gnomAD v4: 14-35404623-G-T
• MyVariant Identifiers: chr14:g.35873829G>T (hg19) ; chr14:g.35404623G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.35404623G>T , CM000676.2:g.35404623G>T	GRCh38
NC_000014.8:g.35873829G>T , CM000676.1:g.35873829G>T	GRCh37
NC_000014.7:g.34943580G>T	NCBI36
NG_007571.1:g.5116C>A , LRG_89:g.5116C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000553342.2:c.22C>A	ENSP00000451281.2:p.Pro8Thr
ENST00000557459.2:n.120C>A
ENST00000697957.1:n.127C>A
ENST00000697958.1:n.120C>A
ENST00000697959.1:n.127C>A
ENST00000697960.1:n.107C>A
ENST00000697961.1:c.22C>A	ENSP00000513487.1:p.Pro8Thr
ENST00000697966.1:n.49-9C>A
ENST00000216797.10:c.22C>A MANE Select	ENSP00000216797.6:p.Pro8Thr
ENST00000216797.9:c.22C>A	ENSP00000216797.5:p.Pro8Thr
ENST00000553342.1:c.22C>A	ENSP00000451281.1:p.Pro8Thr
ENST00000554001.5:c.22C>A	ENSP00000450537.1:p.Pro8Thr
ENST00000555629.1:n.127C>A
ENST00000557100.5:n.78C>A
ENST00000557140.5:c.22C>A	ENSP00000451257.1:p.Pro8Thr
ENST00000557459.1:n.120C>A
NM_020529.2:c.22C>A , LRG_89t1:c.22C>A	NP_065390.1:p.Pro8Thr
NM_020529.3:c.22C>A MANE Select	NP_065390.1:p.Pro8Thr