Canonical Allele Identifier: CA1630856045
Community Standard Title: NM_020529.3(NFKBIA):c.81C= (p.Asp27=)
Gene: NFKBIA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.35404564G= , CM000676.2:g.35404564G= GRCh38
NC_000014.8:g.35873770G= , CM000676.1:g.35873770G= GRCh37
NC_000014.7:g.34943521G= NCBI36
NG_007571.1:g.5175C= , LRG_89:g.5175C=

Transcript Alleles

HGVS Amino-acid Change
NM_020529.3:c.81C= MANE Select NP_065390.1:p.Asp27=
ENST00000216797.10:c.81C= MANE Select ENSP00000216797.6:p.Asp27=
NM_020529.2:c.81C= , LRG_89t1:c.81C= NP_065390.1:p.Asp27=
ENST00000216797.9:c.81C= ENSP00000216797.5:p.Asp27=
ENST00000553342.1:c.81C= ENSP00000451281.1:p.Asp27=
ENST00000553342.2:c.81C= ENSP00000451281.2:p.Asp27=
ENST00000554001.5:c.81C= ENSP00000450537.1:p.Asp27=
ENST00000555629.1:n.186C=
ENST00000557100.5:n.137C=
ENST00000557140.5:c.81C= ENSP00000451257.1:p.Asp27=
ENST00000557459.1:n.179C=
ENST00000557459.2:n.179C=
ENST00000697957.1:n.186C=
ENST00000697958.1:n.179C=
ENST00000697959.1:n.186C=
ENST00000697960.1:n.166C=
ENST00000697961.1:c.81C= ENSP00000513487.1:p.Asp27=
ENST00000697966.1:n.99C=