Canonical Allele Identifier: CA357960192

Gene: NFKB1

Linked Data - Predicted Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.102580641T>C , CM000666.2:g.102580641T>C	GRCh38
NC_000004.11:g.103501798T>C , CM000666.1:g.103501798T>C	GRCh37
NC_000004.10:g.103720836T>C	NCBI36
NG_050628.1:g.84313T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000507079.6:c.859+2T>C	ENSP00000426147.2:n.859+2T>C
ENST00000509165.2:c.835+2T>C	ENSP00000423877.2:n.835+2T>C
ENST00000697794.1:c.*476+2T>C	ENSP00000513443.1:n.*476+2T>C
ENST00000697799.1:n.332+2T>C
ENST00000697800.1:n.46+2T>C
ENST00000226574.9:c.835+2T>C MANE Select	ENSP00000226574.4:n.835+2T>C
ENST00000652569.1:c.749+2T>C
ENST00000652619.1:c.856+2T>C	ENSP00000499031.1:n.856+2T>C
ENST00000226574.8:c.835+2T>C	ENSP00000226574.4:n.835+2T>C
ENST00000394820.8:c.832+2T>C	ENSP00000378297.4:n.832+2T>C
ENST00000505458.5:c.832+2T>C	ENSP00000424790.1:n.832+2T>C
ENST00000508584.1:c.214+2T>C	ENSP00000424815.1:n.214+2T>C
ENST00000600343.5:c.292+2T>C	ENSP00000469340.1:n.292+2T>C
NM_001165412.1:c.832+2T>C	NP_001158884.1:n.832+2T>C
NM_003998.3:c.835+2T>C	NP_003989.2:n.835+2T>C
XM_011532006.1:c.856+2T>C	XP_011530308.1:n.856+2T>C
XM_011532007.1:c.832+2T>C	XP_011530309.1:n.832+2T>C
XM_011532008.1:c.676+2T>C	XP_011530310.1:n.676+2T>C
XM_011532009.1:c.439+2T>C	XP_011530311.1:n.439+2T>C
NM_001319226.1:c.832+2T>C	NP_001306155.1:n.832+2T>C
XM_011532006.2:c.856+2T>C	XP_011530308.1:n.856+2T>C
XM_024454067.1:c.859+2T>C	XP_024309835.1:n.859+2T>C
XM_024454068.1:c.835+2T>C	XP_024309836.1:n.835+2T>C
XM_024454069.1:c.700+2T>C	XP_024309837.1:n.700+2T>C
NM_003998.4:c.835+2T>C MANE Select	NP_003989.2:n.835+2T>C
NM_001165412.2:c.832+2T>C	NP_001158884.1:n.832+2T>C
NM_001319226.2:c.832+2T>C	NP_001306155.1:n.832+2T>C
NM_001382625.1:c.835+2T>C	NP_001369554.1:n.835+2T>C
NM_001382626.1:c.835+2T>C	NP_001369555.1:n.835+2T>C
NM_001382627.1:c.832+2T>C	NP_001369556.1:n.832+2T>C
NM_001382628.1:c.793+2T>C	NP_001369557.1:n.793+2T>C