Canonical Allele Identifier: CA1481448735

Gene: NFKB1

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.102600814C= , CM000666.2:g.102600814C=	GRCh38
NC_000004.11:g.103521971C= , CM000666.1:g.103521971C=	GRCh37
NC_000004.10:g.103741009C=	NCBI36
NG_050628.1:g.104486C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000507079.6:c.1662-81C=	ENSP00000426147.2:n.1662-81C=
ENST00000509165.2:c.1638-81C=	ENSP00000423877.2:n.1638-81C=
ENST00000697794.1:c.*1279-81C=	ENSP00000513443.1:n.*1279-81C=
ENST00000697799.1:n.1135-81C=
ENST00000698233.1:n.1367-81C=
ENST00000226574.9:c.1638-81C= MANE Select	ENSP00000226574.4:n.1638-81C=
ENST00000652569.1:c.1614-81C=
ENST00000652619.1:c.*165-81C=	ENSP00000499031.1:n.*165-81C=
ENST00000226574.8:c.1638-81C=	ENSP00000226574.4:n.1638-81C=
ENST00000394820.8:c.1635-81C=	ENSP00000378297.4:n.1635-81C=
ENST00000505458.5:c.1635-81C=	ENSP00000424790.1:n.1635-81C=
ENST00000600343.5:c.1095-81C=	ENSP00000469340.1:n.1095-81C=
NM_001165412.1:c.1635-81C=	NP_001158884.1:n.1635-81C=
NM_003998.3:c.1638-81C=	NP_003989.2:n.1638-81C=
XM_011532006.1:c.1659-81C=	XP_011530308.1:n.1659-81C=
XM_011532007.1:c.1635-81C=	XP_011530309.1:n.1635-81C=
XM_011532008.1:c.1479-81C=	XP_011530310.1:n.1479-81C=
XM_011532009.1:c.1242-81C=	XP_011530311.1:n.1242-81C=
XR_939027.1:n.2592-1079G=
NM_001319226.1:c.1635-81C=	NP_001306155.1:n.1635-81C=
XM_011532006.2:c.1659-81C=	XP_011530308.1:n.1659-81C=
XM_024454067.1:c.1662-81C=	XP_024309835.1:n.1662-81C=
XM_024454068.1:c.1638-81C=	XP_024309836.1:n.1638-81C=
XM_024454069.1:c.1503-81C=	XP_024309837.1:n.1503-81C=
XR_001741780.1:n.2578-1079G=
NM_003998.4:c.1638-81C= MANE Select	NP_003989.2:n.1638-81C=
NM_001165412.2:c.1635-81C=	NP_001158884.1:n.1635-81C=
NM_001319226.2:c.1635-81C=	NP_001306155.1:n.1635-81C=
NM_001382625.1:c.1638-81C=	NP_001369554.1:n.1638-81C=
NM_001382626.1:c.1638-81C=	NP_001369555.1:n.1638-81C=
NM_001382627.1:c.1635-81C=	NP_001369556.1:n.1635-81C=
NM_001382628.1:c.1596-81C=	NP_001369557.1:n.1596-81C=