Canonical Allele Identifier: CA1481407571

Gene: NFKB1

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.102501364G= , CM000666.2:g.102501364G=	GRCh38
NC_000004.11:g.103422521G= , CM000666.1:g.103422521G=	GRCh37
NC_000004.10:g.103641553G=	NCBI36
NG_050628.1:g.5036G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000507079.6:c.-478G=	ENSP00000426147.2:n.-478G=
ENST00000226574.9:c.-432G= MANE Select	ENSP00000226574.4:n.-432G=
ENST00000226574.8:c.-432G=	ENSP00000226574.4:n.-432G=
ENST00000394820.8:c.-432G=	ENSP00000378297.4:n.-432G=
NM_001165412.1:c.-432G=	NP_001158884.1:n.-432G=
NM_003998.3:c.-432G=	NP_003989.2:n.-432G=
XM_011532467.1:c.528C=	XP_011530769.1:p.Cys176=
NR_136202.1:n.48+1075C=
XM_024454067.1:c.-478G=	XP_024309835.1:n.-478G=
XM_024454069.1:c.-478G=	XP_024309837.1:n.-478G=
NM_003998.4:c.-432G= MANE Select	NP_003989.2:n.-432G=
NM_001165412.2:c.-432G=	NP_001158884.1:n.-432G=
NM_001382626.1:c.-502G=	NP_001369555.1:n.-502G=
NM_001382627.1:c.-502G=	NP_001369556.1:n.-502G=
NM_001382628.1:c.-425G=	NP_001369557.1:n.-425G=