Canonical Allele Identifier: CA2671575273

Gene: NFKB1

Linked Data

• gnomAD v4: 4-102501423-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.102501423C>A , CM000666.2:g.102501423C>A	GRCh38
NC_000004.11:g.103422580C>A , CM000666.1:g.103422580C>A	GRCh37
NC_000004.10:g.103641612C>A	NCBI36
NG_050628.1:g.5095C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000507079.6:c.-419C>A	ENSP00000426147.2:n.-419C>A
ENST00000226574.9:c.-373C>A MANE Select	ENSP00000226574.4:n.-373C>A
ENST00000652619.1:c.-419C>A	ENSP00000499031.1:n.-419C>A
ENST00000226574.8:c.-373C>A	ENSP00000226574.4:n.-373C>A
ENST00000394820.8:c.-373C>A	ENSP00000378297.4:n.-373C>A
NM_001165412.1:c.-373C>A	NP_001158884.1:n.-373C>A
NM_003998.3:c.-373C>A	NP_003989.2:n.-373C>A
XM_011532467.1:c.469G>T	XP_011530769.1:p.Ala157Ser
NR_136202.1:n.48+1016G>T
XM_024454067.1:c.-419C>A	XP_024309835.1:n.-419C>A
XM_024454069.1:c.-419C>A	XP_024309837.1:n.-419C>A
NM_003998.4:c.-373C>A MANE Select	NP_003989.2:n.-373C>A
NM_001165412.2:c.-373C>A	NP_001158884.1:n.-373C>A
NM_001382626.1:c.-443C>A	NP_001369555.1:n.-443C>A
NM_001382627.1:c.-443C>A	NP_001369556.1:n.-443C>A
NM_001382628.1:c.-366C>A	NP_001369557.1:n.-366C>A