Canonical Allele Identifier: CA705268037

Gene: NFKBIA

Linked Data

• dbSNP Id: rs1362967644
• MyVariant Identifiers: chr14:g.35870822_35870825del (hg19) ; chr14:g.35401616_35401619del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.35401618_35401621del , CM000676.2:g.35401618_35401621del	GRCh38
NC_000014.8:g.35870824_35870827del , CM000676.1:g.35870824_35870827del	GRCh37
NC_000014.7:g.34940575_34940578del	NCBI36
NG_007571.1:g.8120_8123del , LRG_89:g.8120_8123del

Transcript Alleles

HGVS	Amino-acid change
ENST00000553342.2:c.*394_*397del	ENSP00000451281.2:n.*394_*397del
ENST00000697954.1:n.1557_1560del
ENST00000697955.1:n.1596_1599del
ENST00000697956.1:n.1624_1627del
ENST00000697957.1:n.1743_1746del
ENST00000697958.1:n.2398_2401del
ENST00000697959.1:n.2076_2079del
ENST00000697960.1:n.2492_2495del
ENST00000697961.1:c.*763_*766del	ENSP00000513487.1:n.*763_*766del
ENST00000216797.10:c.*394_*397del MANE Select	ENSP00000216797.6:n.*394_*397del
ENST00000216797.9:c.*394_*397del	ENSP00000216797.5:n.*394_*397del
ENST00000554001.5:c.*990_*993del	ENSP00000450537.1:n.*990_*993del
ENST00000557140.5:c.*394_*397del	ENSP00000451257.1:n.*394_*397del
ENST00000557389.1:c.*394_*397del	ENSP00000450514.1:n.*394_*397del
NM_020529.2:c.*394_*397del , LRG_89t1:c.*394_*397del	NP_065390.1:n.*394_*397del
NM_020529.3:c.*394_*397del MANE Select	NP_065390.1:n.*394_*397del