Canonical Allele Identifier: CA649292161

Gene: NFKB1

Linked Data

• COSMIC: COSN9582303

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.102532804G>C , CM000666.2:g.102532804G>C	GRCh38
NC_000004.11:g.103453961G>C , CM000666.1:g.103453961G>C	GRCh37
NC_000004.10:g.103672991G>C	NCBI36
NG_050628.1:g.36476G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000507079.6:c.143-1041G>C	ENSP00000426147.2:n.143-1041G>C
ENST00000509165.2:c.119-1041G>C	ENSP00000423877.2:n.119-1041G>C
ENST00000697793.1:n.257+2890G>C
ENST00000697794.1:c.118+2890G>C	ENSP00000513443.1:n.118+2890G>C
ENST00000697796.1:n.395-1041G>C
ENST00000697797.1:n.316-1044G>C
ENST00000697798.1:n.1792-1044G>C
ENST00000226574.9:c.119-1041G>C MANE Select	ENSP00000226574.4:n.119-1041G>C
ENST00000652569.1:c.36-1044G>C
ENST00000652619.1:c.143-1044G>C	ENSP00000499031.1:n.143-1044G>C
ENST00000226574.8:c.119-1041G>C	ENSP00000226574.4:n.119-1041G>C
ENST00000394820.8:c.119-1044G>C	ENSP00000378297.4:n.119-1044G>C
ENST00000505458.5:c.119-1044G>C	ENSP00000424790.1:n.119-1044G>C
ENST00000507079.5:c.143-1041G>C	ENSP00000426147.1:n.143-1041G>C
ENST00000509165.1:c.119-1041G>C	ENSP00000423877.1:n.119-1041G>C
ENST00000511926.5:c.143-1044G>C	ENSP00000420904.1:n.143-1044G>C
NM_001165412.1:c.119-1044G>C	NP_001158884.1:n.119-1044G>C
NM_003998.3:c.119-1041G>C	NP_003989.2:n.119-1041G>C
XM_011532006.1:c.143-1044G>C	XP_011530308.1:n.143-1044G>C
XM_011532007.1:c.119-1044G>C	XP_011530309.1:n.119-1044G>C
XM_011532008.1:c.119-1041G>C	XP_011530310.1:n.119-1041G>C
XM_011532009.1:c.-238+2890G>C	XP_011530311.1:n.-238+2890G>C
NM_001319226.1:c.119-1044G>C	NP_001306155.1:n.119-1044G>C
XM_011532006.2:c.143-1044G>C	XP_011530308.1:n.143-1044G>C
XM_024454067.1:c.143-1041G>C	XP_024309835.1:n.143-1041G>C
XM_024454068.1:c.119-1041G>C	XP_024309836.1:n.119-1041G>C
XM_024454069.1:c.143-1041G>C	XP_024309837.1:n.143-1041G>C
NM_003998.4:c.119-1041G>C MANE Select	NP_003989.2:n.119-1041G>C
NM_001165412.2:c.119-1044G>C	NP_001158884.1:n.119-1044G>C
NM_001319226.2:c.119-1044G>C	NP_001306155.1:n.119-1044G>C
NM_001382625.1:c.119-1041G>C	NP_001369554.1:n.119-1041G>C
NM_001382626.1:c.119-1041G>C	NP_001369555.1:n.119-1041G>C
NM_001382627.1:c.119-1044G>C	NP_001369556.1:n.119-1044G>C
NM_001382628.1:c.80-1044G>C	NP_001369557.1:n.80-1044G>C