Canonical Allele Identifier: CA2624566859

Gene: NFKBIA

Linked Data

• gnomAD v4: 14-35401660-T-TG

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.35401662dup , CM000676.2:g.35401662dup	GRCh38
NC_000014.8:g.35870868dup , CM000676.1:g.35870868dup	GRCh37
NC_000014.7:g.34940619dup	NCBI36
NG_007571.1:g.8078dup , LRG_89:g.8078dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000553342.2:c.*352dup	ENSP00000451281.2:n.*352dup
ENST00000697954.1:n.1515dup
ENST00000697955.1:n.1554dup
ENST00000697956.1:n.1582dup
ENST00000697957.1:n.1701dup
ENST00000697958.1:n.2356dup
ENST00000697959.1:n.2034dup
ENST00000697960.1:n.2450dup
ENST00000697961.1:c.*721dup	ENSP00000513487.1:n.*721dup
ENST00000216797.10:c.*352dup MANE Select	ENSP00000216797.6:n.*352dup
ENST00000216797.9:c.*352dup	ENSP00000216797.5:n.*352dup
ENST00000554001.5:c.*948dup	ENSP00000450537.1:n.*948dup
ENST00000557140.5:c.*352dup	ENSP00000451257.1:n.*352dup
ENST00000557389.1:c.*352dup	ENSP00000450514.1:n.*352dup
NM_020529.2:c.*352dup , LRG_89t1:c.*352dup	NP_065390.1:n.*352dup
NM_020529.3:c.*352dup MANE Select	NP_065390.1:n.*352dup