Canonical Allele Identifier: CA7155473

Gene: NFKBIA

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.35403288G>A , CM000676.2:g.35403288G>A	GRCh38
NC_000014.8:g.35872494G>A , CM000676.1:g.35872494G>A	GRCh37
NC_000014.7:g.34942245G>A	NCBI36
NG_007571.1:g.6451C>T , LRG_89:g.6451C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_020529.3:c.409C>T MANE Select	NP_065390.1:p.Pro137Ser
ENST00000216797.10:c.409C>T MANE Select	ENSP00000216797.6:p.Pro137Ser
NM_020529.2:c.409C>T , LRG_89t1:c.409C>T	NP_065390.1:p.Pro137Ser
ENST00000216797.9:c.409C>T	ENSP00000216797.5:p.Pro137Ser
ENST00000553342.2:c.337C>T	ENSP00000451281.2:p.Pro113Ser
ENST00000554001.5:c.*51C>T	ENSP00000450537.1:n.*51C>T
ENST00000556664.1:n.143C>T
ENST00000557100.5:n.465C>T
ENST00000557140.5:c.409C>T	ENSP00000451257.1:p.Pro137Ser
ENST00000557389.1:c.139C>T	ENSP00000450514.1:p.Pro47Ser
ENST00000557459.1:n.507C>T
ENST00000557459.2:n.507C>T
ENST00000697954.1:n.221C>T
ENST00000697955.1:n.367C>T
ENST00000697956.1:n.288C>T
ENST00000697957.1:n.514C>T
ENST00000697958.1:n.836C>T
ENST00000697959.1:n.514C>T
ENST00000697960.1:n.823C>T
ENST00000697961.1:c.409C>T	ENSP00000513487.1:p.Pro137Ser
ENST00000697962.1:c.139C>T	ENSP00000513488.1:p.Pro47Ser
ENST00000697966.1:n.427C>T