Canonical Allele Identifier: CA2671576791

Gene: NFKB1

Linked Data

• gnomAD v4: 4-102537581-CAGATTACTCTCCACACATGCATAGCATGAGAGGTTCCATGGGCTTAGGTACCTGGCTTTTTAGCCATATCTTAGTGTACAAATATCAATTAATACCATTTTTCGTAGTA-C

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.102537589_102537697del , CM000666.2:g.102537589_102537697del	GRCh38
NC_000004.11:g.103458746_103458854del , CM000666.1:g.103458746_103458854del	GRCh37
NG_050628.1:g.41261_41369del

Transcript Alleles

HGVS	Amino-acid change
ENST00000507079.6:c.184-269_184-161del	ENSP00000426147.2:n.184-269_184-161del
ENST00000509165.2:c.160-269_160-161del	ENSP00000423877.2:n.160-269_160-161del
ENST00000697793.1:n.258-269_258-161del
ENST00000697794.1:c.118+7675_118+7783del	ENSP00000513443.1:n.118+7675_118+7783del
ENST00000697796.1:n.436-269_436-161del
ENST00000697797.1:n.354-269_354-161del
ENST00000697798.1:n.5533_5641del
ENST00000226574.9:c.160-269_160-161del MANE Select	ENSP00000226574.4:n.160-269_160-161del
ENST00000652569.1:c.74-269_74-161del
ENST00000652619.1:c.181-269_181-161del	ENSP00000499031.1:n.181-269_181-161del
ENST00000226574.8:c.160-269_160-161del	ENSP00000226574.4:n.160-269_160-161del
ENST00000394820.8:c.157-269_157-161del	ENSP00000378297.4:n.157-269_157-161del
ENST00000505458.5:c.157-269_157-161del	ENSP00000424790.1:n.157-269_157-161del
ENST00000507079.5:c.184-269_184-161del	ENSP00000426147.1:n.184-269_184-161del
ENST00000509165.1:c.160-269_160-161del	ENSP00000423877.1:n.160-269_160-161del
ENST00000511926.5:c.181-269_181-161del	ENSP00000420904.1:n.181-269_181-161del
NM_001165412.1:c.157-269_157-161del	NP_001158884.1:n.157-269_157-161del
NM_003998.3:c.160-269_160-161del	NP_003989.2:n.160-269_160-161del
XM_011532006.1:c.181-269_181-161del	XP_011530308.1:n.181-269_181-161del
XM_011532007.1:c.157-269_157-161del	XP_011530309.1:n.157-269_157-161del
XM_011532008.1:c.160-269_160-161del	XP_011530310.1:n.160-269_160-161del
XM_011532009.1:c.-237-269_-237-161del	XP_011530311.1:n.-237-269_-237-161del
NM_001319226.1:c.157-269_157-161del	NP_001306155.1:n.157-269_157-161del
XM_011532006.2:c.181-269_181-161del	XP_011530308.1:n.181-269_181-161del
XM_024454067.1:c.184-269_184-161del	XP_024309835.1:n.184-269_184-161del
XM_024454068.1:c.160-269_160-161del	XP_024309836.1:n.160-269_160-161del
XM_024454069.1:c.184-269_184-161del	XP_024309837.1:n.184-269_184-161del
NM_003998.4:c.160-269_160-161del MANE Select	NP_003989.2:n.160-269_160-161del
NM_001165412.2:c.157-269_157-161del	NP_001158884.1:n.157-269_157-161del
NM_001319226.2:c.157-269_157-161del	NP_001306155.1:n.157-269_157-161del
NM_001382625.1:c.160-269_160-161del	NP_001369554.1:n.160-269_160-161del
NM_001382626.1:c.160-269_160-161del	NP_001369555.1:n.160-269_160-161del
NM_001382627.1:c.157-269_157-161del	NP_001369556.1:n.157-269_157-161del
NM_001382628.1:c.118-269_118-161del	NP_001369557.1:n.118-269_118-161del