Canonical Allele Identifier: CA7155530

Gene: NFKBIA

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.35403727T>C , CM000676.2:g.35403727T>C	GRCh38
NC_000014.8:g.35872933T>C , CM000676.1:g.35872933T>C	GRCh37
NC_000014.7:g.34942684T>C	NCBI36
NG_007571.1:g.6012A>G , LRG_89:g.6012A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_020529.3:c.299A>G MANE Select	NP_065390.1:p.Asp100Gly
ENST00000216797.10:c.299A>G MANE Select	ENSP00000216797.6:p.Asp100Gly
NM_020529.2:c.299A>G , LRG_89t1:c.299A>G	NP_065390.1:p.Asp100Gly
ENST00000216797.9:c.299A>G	ENSP00000216797.5:p.Asp100Gly
ENST00000553342.2:c.227A>G	ENSP00000451281.2:p.Asp76Gly
ENST00000554001.5:c.228-367A>G	ENSP00000450537.1:n.228-367A>G
ENST00000555629.1:n.404A>G
ENST00000557100.5:n.355A>G
ENST00000557140.5:c.299A>G	ENSP00000451257.1:p.Asp100Gly
ENST00000557389.1:c.29A>G	ENSP00000450514.1:p.Asp10Gly
ENST00000557459.1:n.397A>G
ENST00000557459.2:n.397A>G
ENST00000697956.1:n.178A>G
ENST00000697957.1:n.404A>G
ENST00000697958.1:n.397A>G
ENST00000697959.1:n.404A>G
ENST00000697960.1:n.384A>G
ENST00000697961.1:c.299A>G	ENSP00000513487.1:p.Asp100Gly
ENST00000697962.1:c.29A>G	ENSP00000513488.1:p.Asp10Gly
ENST00000697966.1:n.317A>G