Canonical Allele Identifier: CA389455464

Gene: NFKBIA

Linked Data

• MyVariant Identifiers: chr14:g.35873819C>G (hg19) ; chr14:g.35404613C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.35404613C>G , CM000676.2:g.35404613C>G	GRCh38
NC_000014.8:g.35873819C>G , CM000676.1:g.35873819C>G	GRCh37
NC_000014.7:g.34943570C>G	NCBI36
NG_007571.1:g.5126G>C , LRG_89:g.5126G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000553342.2:c.32G>C	ENSP00000451281.2:p.Trp11Ser
ENST00000557459.2:n.130G>C
ENST00000697957.1:n.137G>C
ENST00000697958.1:n.130G>C
ENST00000697959.1:n.137G>C
ENST00000697960.1:n.117G>C
ENST00000697961.1:c.32G>C	ENSP00000513487.1:p.Trp11Ser
ENST00000697966.1:n.50G>C
ENST00000216797.10:c.32G>C MANE Select	ENSP00000216797.6:p.Trp11Ser
ENST00000216797.9:c.32G>C	ENSP00000216797.5:p.Trp11Ser
ENST00000553342.1:c.32G>C	ENSP00000451281.1:p.Trp11Ser
ENST00000554001.5:c.32G>C	ENSP00000450537.1:p.Trp11Ser
ENST00000555629.1:n.137G>C
ENST00000557100.5:n.88G>C
ENST00000557140.5:c.32G>C	ENSP00000451257.1:p.Trp11Ser
ENST00000557459.1:n.130G>C
NM_020529.2:c.32G>C , LRG_89t1:c.32G>C	NP_065390.1:p.Trp11Ser
NM_020529.3:c.32G>C MANE Select	NP_065390.1:p.Trp11Ser