Canonical Allele Identifier: CA3026042

Gene: NFKB1

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.102584804C>T , CM000666.2:g.102584804C>T	GRCh38
NC_000004.11:g.103505961C>T , CM000666.1:g.103505961C>T	GRCh37
NC_000004.10:g.103724999C>T	NCBI36
NG_050628.1:g.88476C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000507079.6:c.1074C>T	ENSP00000426147.2:p.Tyr358=
ENST00000509165.2:c.1050C>T	ENSP00000423877.2:p.Tyr350=
ENST00000697794.1:c.*691C>T	ENSP00000513443.1:n.*691C>T
ENST00000697799.1:n.547C>T
ENST00000697800.1:n.189C>T
ENST00000226574.9:c.1050C>T MANE Select	ENSP00000226574.4:p.Tyr350=
ENST00000652569.1:c.1026C>T
ENST00000652619.1:c.1071C>T	ENSP00000499031.1:p.Tyr357=
ENST00000226574.8:c.1050C>T	ENSP00000226574.4:p.Tyr350=
ENST00000394820.8:c.1047C>T	ENSP00000378297.4:p.Tyr349=
ENST00000505458.5:c.1047C>T	ENSP00000424790.1:p.Tyr349=
ENST00000508584.1:c.429C>T	ENSP00000424815.1:p.Tyr143=
ENST00000600343.5:c.507C>T	ENSP00000469340.1:p.Tyr169=
NM_001165412.1:c.1047C>T	NP_001158884.1:p.Tyr349=
NM_003998.3:c.1050C>T	NP_003989.2:p.Tyr350=
XM_011532006.1:c.1071C>T	XP_011530308.1:p.Tyr357=
XM_011532007.1:c.1047C>T	XP_011530309.1:p.Tyr349=
XM_011532008.1:c.891C>T	XP_011530310.1:p.Tyr297=
XM_011532009.1:c.654C>T	XP_011530311.1:p.Tyr218=
NM_001319226.1:c.1047C>T	NP_001306155.1:p.Tyr349=
XM_011532006.2:c.1071C>T	XP_011530308.1:p.Tyr357=
XM_024454067.1:c.1074C>T	XP_024309835.1:p.Tyr358=
XM_024454068.1:c.1050C>T	XP_024309836.1:p.Tyr350=
XM_024454069.1:c.915C>T	XP_024309837.1:p.Tyr305=
NM_003998.4:c.1050C>T MANE Select	NP_003989.2:p.Tyr350=
NM_001165412.2:c.1047C>T	NP_001158884.1:p.Tyr349=
NM_001319226.2:c.1047C>T	NP_001306155.1:p.Tyr349=
NM_001382625.1:c.1050C>T	NP_001369554.1:p.Tyr350=
NM_001382626.1:c.1050C>T	NP_001369555.1:p.Tyr350=
NM_001382627.1:c.1047C>T	NP_001369556.1:p.Tyr349=
NM_001382628.1:c.1008C>T	NP_001369557.1:p.Tyr336=