Canonical Allele Identifier: CA1066154947

Gene: NFKB1

Linked Data

• dbSNP Id: rs1741387144
• gnomAD v3: 4-102532849-ATGC-A
• gnomAD v4: 4-102532849-ATGC-A

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.102532850_102532852del , CM000666.2:g.102532850_102532852del	GRCh38
NC_000004.11:g.103454007_103454009del , CM000666.1:g.103454007_103454009del	GRCh37
NC_000004.10:g.103673037_103673039del	NCBI36
NG_050628.1:g.36522_36524del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000507079.6:c.143-995_143-993del	ENSP00000426147.2:n.143-995_143-993del
ENST00000509165.2:c.119-995_119-993del	ENSP00000423877.2:n.119-995_119-993del
ENST00000697793.1:n.257+2936_257+2938del
ENST00000697794.1:c.118+2936_118+2938del	ENSP00000513443.1:n.118+2936_118+2938del
ENST00000697796.1:n.395-995_395-993del
ENST00000697797.1:n.316-998_316-996del
ENST00000697798.1:n.1792-998_1792-996del
ENST00000226574.9:c.119-995_119-993del MANE Select	ENSP00000226574.4:n.119-995_119-993del
ENST00000652569.1:c.36-998_36-996del
ENST00000652619.1:c.143-998_143-996del	ENSP00000499031.1:n.143-998_143-996del
ENST00000226574.8:c.119-995_119-993del	ENSP00000226574.4:n.119-995_119-993del
ENST00000394820.8:c.119-998_119-996del	ENSP00000378297.4:n.119-998_119-996del
ENST00000505458.5:c.119-998_119-996del	ENSP00000424790.1:n.119-998_119-996del
ENST00000507079.5:c.143-995_143-993del	ENSP00000426147.1:n.143-995_143-993del
ENST00000509165.1:c.119-995_119-993del	ENSP00000423877.1:n.119-995_119-993del
ENST00000511926.5:c.143-998_143-996del	ENSP00000420904.1:n.143-998_143-996del
NM_001165412.1:c.119-998_119-996del	NP_001158884.1:n.119-998_119-996del
NM_003998.3:c.119-995_119-993del	NP_003989.2:n.119-995_119-993del
XM_011532006.1:c.143-998_143-996del	XP_011530308.1:n.143-998_143-996del
XM_011532007.1:c.119-998_119-996del	XP_011530309.1:n.119-998_119-996del
XM_011532008.1:c.119-995_119-993del	XP_011530310.1:n.119-995_119-993del
XM_011532009.1:c.-238+2936_-238+2938del	XP_011530311.1:n.-238+2936_-238+2938del
NM_001319226.1:c.119-998_119-996del	NP_001306155.1:n.119-998_119-996del
XM_011532006.2:c.143-998_143-996del	XP_011530308.1:n.143-998_143-996del
XM_024454067.1:c.143-995_143-993del	XP_024309835.1:n.143-995_143-993del
XM_024454068.1:c.119-995_119-993del	XP_024309836.1:n.119-995_119-993del
XM_024454069.1:c.143-995_143-993del	XP_024309837.1:n.143-995_143-993del
NM_003998.4:c.119-995_119-993del MANE Select	NP_003989.2:n.119-995_119-993del
NM_001165412.2:c.119-998_119-996del	NP_001158884.1:n.119-998_119-996del
NM_001319226.2:c.119-998_119-996del	NP_001306155.1:n.119-998_119-996del
NM_001382625.1:c.119-995_119-993del	NP_001369554.1:n.119-995_119-993del
NM_001382626.1:c.119-995_119-993del	NP_001369555.1:n.119-995_119-993del
NM_001382627.1:c.119-998_119-996del	NP_001369556.1:n.119-998_119-996del
NM_001382628.1:c.80-998_80-996del	NP_001369557.1:n.80-998_80-996del