Canonical Allele Identifier: CA2671575300

Gene: NFKB1

Linked Data

• gnomAD v4: 4-102501452-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.102501452T>C , CM000666.2:g.102501452T>C	GRCh38
NC_000004.11:g.103422609T>C , CM000666.1:g.103422609T>C	GRCh37
NC_000004.10:g.103641641T>C	NCBI36
NG_050628.1:g.5124T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000507079.6:c.-390T>C	ENSP00000426147.2:n.-390T>C
ENST00000226574.9:c.-344T>C MANE Select	ENSP00000226574.4:n.-344T>C
ENST00000652619.1:c.-390T>C	ENSP00000499031.1:n.-390T>C
ENST00000226574.8:c.-344T>C	ENSP00000226574.4:n.-344T>C
ENST00000394820.8:c.-344T>C	ENSP00000378297.4:n.-344T>C
NM_001165412.1:c.-344T>C	NP_001158884.1:n.-344T>C
NM_003998.3:c.-344T>C	NP_003989.2:n.-344T>C
XM_011532467.1:c.440A>G	XP_011530769.1:p.Asp147Gly
NR_136202.1:n.48+987A>G
XM_024454067.1:c.-390T>C	XP_024309835.1:n.-390T>C
XM_024454069.1:c.-390T>C	XP_024309837.1:n.-390T>C
NM_003998.4:c.-344T>C MANE Select	NP_003989.2:n.-344T>C
NM_001165412.2:c.-344T>C	NP_001158884.1:n.-344T>C
NM_001382626.1:c.-414T>C	NP_001369555.1:n.-414T>C
NM_001382627.1:c.-414T>C	NP_001369556.1:n.-414T>C
NM_001382628.1:c.-337T>C	NP_001369557.1:n.-337T>C