Canonical Allele Identifier: CA705268021

Gene: NFKBIA

Linked Data

• dbSNP Id: rs1207536187
• gnomAD v3: 14-35401596-AG-A
• gnomAD v4: 14-35401596-AG-A
• MyVariant Identifiers: chr14:g.35870803del (hg19) ; chr14:g.35401597del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.35401599del , CM000676.2:g.35401599del	GRCh38
NC_000014.8:g.35870805del , CM000676.1:g.35870805del	GRCh37
NC_000014.7:g.34940556del	NCBI36
NG_007571.1:g.8142del , LRG_89:g.8142del

Transcript Alleles

HGVS	Amino-acid change
ENST00000553342.2:c.*416del	ENSP00000451281.2:n.*416del
ENST00000697954.1:n.1579del
ENST00000697955.1:n.1618del
ENST00000697956.1:n.1646del
ENST00000697957.1:n.1765del
ENST00000697958.1:n.2420del
ENST00000697959.1:n.2098del
ENST00000697960.1:n.2514del
ENST00000697961.1:c.*785del	ENSP00000513487.1:n.*785del
ENST00000216797.10:c.*416del MANE Select	ENSP00000216797.6:n.*416del
ENST00000216797.9:c.*416del	ENSP00000216797.5:n.*416del
ENST00000554001.5:c.*1012del	ENSP00000450537.1:n.*1012del
ENST00000557140.5:c.*416del	ENSP00000451257.1:n.*416del
ENST00000557389.1:c.*416del	ENSP00000450514.1:n.*416del
NM_020529.2:c.*416del , LRG_89t1:c.*416del	NP_065390.1:n.*416del
NM_020529.3:c.*416del MANE Select	NP_065390.1:n.*416del