Canonical Allele Identifier: CA1481398894

Gene: NFKB1

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.102523365_102523366delinsCT , CM000666.2:g.102523365_102523366delinsCT	GRCh38
NC_000004.11:g.103444522_103444523delinsCT , CM000666.1:g.103444522_103444523delinsCT	GRCh37
NC_000004.10:g.103663552_103663553delinsCT	NCBI36
NG_050628.1:g.27037_27038delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000507079.6:c.18-2147_18-2146delinsCT	ENSP00000426147.2:n.18-2147_18-2146delinsCT
ENST00000509165.2:c.-7-2147_-7-2146delinsCT	ENSP00000423877.2:n.-7-2147_-7-2146delinsCT
ENST00000697793.1:n.179-6471_179-6470delinsCT
ENST00000697794.1:c.-7-2147_-7-2146delinsCT	ENSP00000513443.1:n.-7-2147_-7-2146delinsCT
ENST00000697795.1:n.47-2147_47-2146delinsCT
ENST00000697796.1:n.276-2153_276-2152delinsCT
ENST00000697797.1:n.197-2153_197-2152delinsCT
ENST00000226574.9:c.-7-2147_-7-2146delinsCT MANE Select	ENSP00000226574.4:n.-7-2147_-7-2146delinsCT
ENST00000652619.1:c.18-2147_18-2146delinsCT	ENSP00000499031.1:n.18-2147_18-2146delinsCT
ENST00000226574.8:c.-7-2147_-7-2146delinsCT	ENSP00000226574.4:n.-7-2147_-7-2146delinsCT
ENST00000394820.8:c.-7-2147_-7-2146delinsCT	ENSP00000378297.4:n.-7-2147_-7-2146delinsCT
ENST00000505458.5:c.-7-2147_-7-2146delinsCT	ENSP00000424790.1:n.-7-2147_-7-2146delinsCT
ENST00000507079.5:c.18-2147_18-2146delinsCT	ENSP00000426147.1:n.18-2147_18-2146delinsCT
ENST00000509165.1:c.-7-2147_-7-2146delinsCT	ENSP00000423877.1:n.-7-2147_-7-2146delinsCT
ENST00000511926.5:c.18-2147_18-2146delinsCT	ENSP00000420904.1:n.18-2147_18-2146delinsCT
NM_001165412.1:c.-7-2147_-7-2146delinsCT	NP_001158884.1:n.-7-2147_-7-2146delinsCT
NM_003998.3:c.-7-2147_-7-2146delinsCT	NP_003989.2:n.-7-2147_-7-2146delinsCT
XM_011532006.1:c.18-2147_18-2146delinsCT	XP_011530308.1:n.18-2147_18-2146delinsCT
XM_011532007.1:c.-7-2147_-7-2146delinsCT	XP_011530309.1:n.-7-2147_-7-2146delinsCT
NM_001319226.1:c.-7-2147_-7-2146delinsCT	NP_001306155.1:n.-7-2147_-7-2146delinsCT
XM_011532006.2:c.18-2147_18-2146delinsCT	XP_011530308.1:n.18-2147_18-2146delinsCT
XM_024454067.1:c.18-2147_18-2146delinsCT	XP_024309835.1:n.18-2147_18-2146delinsCT
XM_024454068.1:c.-7-2147_-7-2146delinsCT	XP_024309836.1:n.-7-2147_-7-2146delinsCT
XM_024454069.1:c.18-2147_18-2146delinsCT	XP_024309837.1:n.18-2147_18-2146delinsCT
NM_003998.4:c.-7-2147_-7-2146delinsCT MANE Select	NP_003989.2:n.-7-2147_-7-2146delinsCT
NM_001165412.2:c.-7-2147_-7-2146delinsCT	NP_001158884.1:n.-7-2147_-7-2146delinsCT
NM_001319226.2:c.-7-2147_-7-2146delinsCT	NP_001306155.1:n.-7-2147_-7-2146delinsCT
NM_001382625.1:c.-7-2147_-7-2146delinsCT	NP_001369554.1:n.-7-2147_-7-2146delinsCT
NM_001382626.1:c.-7-2147_-7-2146delinsCT	NP_001369555.1:n.-7-2147_-7-2146delinsCT
NM_001382627.1:c.-7-2147_-7-2146delinsCT	NP_001369556.1:n.-7-2147_-7-2146delinsCT
NM_001382628.1:c.1-6471_1-6470delinsCT	NP_001369557.1:n.1-6471_1-6470delinsCT