Canonical Allele Identifier: CA1481439558

Gene: NFKB1

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.102579065G= , CM000666.2:g.102579065G=	GRCh38
NC_000004.11:g.103500222G= , CM000666.1:g.103500222G=	GRCh37
NC_000004.10:g.103719260G=	NCBI36
NG_050628.1:g.82737G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000507079.6:c.754+26G=	ENSP00000426147.2:n.754+26G=
ENST00000509165.2:c.730+26G=	ENSP00000423877.2:n.730+26G=
ENST00000697794.1:c.*371+26G=	ENSP00000513443.1:n.*371+26G=
ENST00000226574.9:c.730+26G= MANE Select	ENSP00000226574.4:n.730+26G=
ENST00000652569.1:c.644+26G=
ENST00000652619.1:c.751+26G=	ENSP00000499031.1:n.751+26G=
ENST00000226574.8:c.730+26G=	ENSP00000226574.4:n.730+26G=
ENST00000394820.8:c.727+26G=	ENSP00000378297.4:n.727+26G=
ENST00000505458.5:c.727+26G=	ENSP00000424790.1:n.727+26G=
ENST00000508584.1:c.109+26G=	ENSP00000424815.1:n.109+26G=
ENST00000510638.1:n.574+26G=
ENST00000600343.5:c.187+26G=	ENSP00000469340.1:n.187+26G=
NM_001165412.1:c.727+26G=	NP_001158884.1:n.727+26G=
NM_003998.3:c.730+26G=	NP_003989.2:n.730+26G=
XM_011532006.1:c.751+26G=	XP_011530308.1:n.751+26G=
XM_011532007.1:c.727+26G=	XP_011530309.1:n.727+26G=
XM_011532008.1:c.572-1470G=	XP_011530310.1:n.572-1470G=
XM_011532009.1:c.334+26G=	XP_011530311.1:n.334+26G=
NM_001319226.1:c.727+26G=	NP_001306155.1:n.727+26G=
XM_011532006.2:c.751+26G=	XP_011530308.1:n.751+26G=
XM_024454067.1:c.754+26G=	XP_024309835.1:n.754+26G=
XM_024454068.1:c.730+26G=	XP_024309836.1:n.730+26G=
XM_024454069.1:c.596-1470G=	XP_024309837.1:n.596-1470G=
NM_003998.4:c.730+26G= MANE Select	NP_003989.2:n.730+26G=
NM_001165412.2:c.727+26G=	NP_001158884.1:n.727+26G=
NM_001319226.2:c.727+26G=	NP_001306155.1:n.727+26G=
NM_001382625.1:c.730+26G=	NP_001369554.1:n.730+26G=
NM_001382626.1:c.730+26G=	NP_001369555.1:n.730+26G=
NM_001382627.1:c.727+26G=	NP_001369556.1:n.727+26G=
NM_001382628.1:c.688+26G=	NP_001369557.1:n.688+26G=