Canonical Allele Identifier: CA2624566846

Gene: NFKBIA

Linked Data

• gnomAD v4: 14-35401644-G-A

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.35401644G>A , CM000676.2:g.35401644G>A	GRCh38
NC_000014.8:g.35870850G>A , CM000676.1:g.35870850G>A	GRCh37
NC_000014.7:g.34940601G>A	NCBI36
NG_007571.1:g.8095C>T , LRG_89:g.8095C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000553342.2:c.*369C>T	ENSP00000451281.2:n.*369C>T
ENST00000697954.1:n.1532C>T
ENST00000697955.1:n.1571C>T
ENST00000697956.1:n.1599C>T
ENST00000697957.1:n.1718C>T
ENST00000697958.1:n.2373C>T
ENST00000697959.1:n.2051C>T
ENST00000697960.1:n.2467C>T
ENST00000697961.1:c.*738C>T	ENSP00000513487.1:n.*738C>T
ENST00000216797.10:c.*369C>T MANE Select	ENSP00000216797.6:n.*369C>T
ENST00000216797.9:c.*369C>T	ENSP00000216797.5:n.*369C>T
ENST00000554001.5:c.*965C>T	ENSP00000450537.1:n.*965C>T
ENST00000557140.5:c.*369C>T	ENSP00000451257.1:n.*369C>T
ENST00000557389.1:c.*369C>T	ENSP00000450514.1:n.*369C>T
NM_020529.2:c.*369C>T , LRG_89t1:c.*369C>T	NP_065390.1:n.*369C>T
NM_020529.3:c.*369C>T MANE Select	NP_065390.1:n.*369C>T