Canonical Allele Identifier: CA2671578817

Gene: NFKB1

Linked Data

• gnomAD v4: 4-102582754-A-T

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.102582754A>T , CM000666.2:g.102582754A>T	GRCh38
NC_000004.11:g.103503911A>T , CM000666.1:g.103503911A>T	GRCh37
NC_000004.10:g.103722949A>T	NCBI36
NG_050628.1:g.86426A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000507079.6:c.860-112A>T	ENSP00000426147.2:n.860-112A>T
ENST00000509165.2:c.836-112A>T	ENSP00000423877.2:n.836-112A>T
ENST00000697794.1:c.*477-112A>T	ENSP00000513443.1:n.*477-112A>T
ENST00000697799.1:n.333-112A>T
ENST00000697800.1:n.47-112A>T
ENST00000226574.9:c.836-112A>T MANE Select	ENSP00000226574.4:n.836-112A>T
ENST00000652569.1:c.812-112A>T
ENST00000652619.1:c.857-112A>T	ENSP00000499031.1:n.857-112A>T
ENST00000226574.8:c.836-112A>T	ENSP00000226574.4:n.836-112A>T
ENST00000394820.8:c.833-112A>T	ENSP00000378297.4:n.833-112A>T
ENST00000505458.5:c.833-112A>T	ENSP00000424790.1:n.833-112A>T
ENST00000508584.1:c.215-112A>T	ENSP00000424815.1:n.215-112A>T
ENST00000600343.5:c.293-112A>T	ENSP00000469340.1:n.293-112A>T
NM_001165412.1:c.833-112A>T	NP_001158884.1:n.833-112A>T
NM_003998.3:c.836-112A>T	NP_003989.2:n.836-112A>T
XM_011532006.1:c.857-112A>T	XP_011530308.1:n.857-112A>T
XM_011532007.1:c.833-112A>T	XP_011530309.1:n.833-112A>T
XM_011532008.1:c.677-112A>T	XP_011530310.1:n.677-112A>T
XM_011532009.1:c.440-112A>T	XP_011530311.1:n.440-112A>T
NM_001319226.1:c.833-112A>T	NP_001306155.1:n.833-112A>T
XM_011532006.2:c.857-112A>T	XP_011530308.1:n.857-112A>T
XM_024454067.1:c.860-112A>T	XP_024309835.1:n.860-112A>T
XM_024454068.1:c.836-112A>T	XP_024309836.1:n.836-112A>T
XM_024454069.1:c.701-112A>T	XP_024309837.1:n.701-112A>T
NM_003998.4:c.836-112A>T MANE Select	NP_003989.2:n.836-112A>T
NM_001165412.2:c.833-112A>T	NP_001158884.1:n.833-112A>T
NM_001319226.2:c.833-112A>T	NP_001306155.1:n.833-112A>T
NM_001382625.1:c.836-112A>T	NP_001369554.1:n.836-112A>T
NM_001382626.1:c.836-112A>T	NP_001369555.1:n.836-112A>T
NM_001382627.1:c.833-112A>T	NP_001369556.1:n.833-112A>T
NM_001382628.1:c.794-112A>T	NP_001369557.1:n.794-112A>T