Canonical Allele Identifier: CA1481439560

Gene: NFKB1

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.102579072_102579085delinsAAGAATAGACTTCC , CM000666.2:g.102579072_102579085delinsAAGAATAGACTTCC	GRCh38
NC_000004.11:g.103500229_103500242delinsAAGAATAGACTTCC , CM000666.1:g.103500229_103500242delinsAAGAATAGACTTCC	GRCh37
NC_000004.10:g.103719267_103719280delinsAAGAATAGACTTCC	NCBI36
NG_050628.1:g.82744_82757delinsAAGAATAGACTTCC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000507079.6:c.754+33_754+46delinsAAGAATAGACTTCC	ENSP00000426147.2:n.754+33_754+46delinsAAGAATAGACTTCC
ENST00000509165.2:c.730+33_730+46delinsAAGAATAGACTTCC	ENSP00000423877.2:n.730+33_730+46delinsAAGAATAGACTTCC
ENST00000697794.1:c.*371+33_*371+46delinsAAGAATAGACTTCC	ENSP00000513443.1:n.*371+33_*371+46delinsAAGAATAGACTTCC
ENST00000226574.9:c.730+33_730+46delinsAAGAATAGACTTCC MANE Select	ENSP00000226574.4:n.730+33_730+46delinsAAGAATAGACTTCC
ENST00000652569.1:c.644+33_644+46delinsAAGAATAGACTTCC
ENST00000652619.1:c.751+33_751+46delinsAAGAATAGACTTCC	ENSP00000499031.1:n.751+33_751+46delinsAAGAATAGACTTCC
ENST00000226574.8:c.730+33_730+46delinsAAGAATAGACTTCC	ENSP00000226574.4:n.730+33_730+46delinsAAGAATAGACTTCC
ENST00000394820.8:c.727+33_727+46delinsAAGAATAGACTTCC	ENSP00000378297.4:n.727+33_727+46delinsAAGAATAGACTTCC
ENST00000505458.5:c.727+33_727+46delinsAAGAATAGACTTCC	ENSP00000424790.1:n.727+33_727+46delinsAAGAATAGACTTCC
ENST00000508584.1:c.109+33_109+46delinsAAGAATAGACTTCC	ENSP00000424815.1:n.109+33_109+46delinsAAGAATAGACTTCC
ENST00000510638.1:n.574+33_574+46delinsAAGAATAGACTTCC
ENST00000600343.5:c.187+33_187+46delinsAAGAATAGACTTCC	ENSP00000469340.1:n.187+33_187+46delinsAAGAATAGACTTCC
NM_001165412.1:c.727+33_727+46delinsAAGAATAGACTTCC	NP_001158884.1:n.727+33_727+46delinsAAGAATAGACTTCC
NM_003998.3:c.730+33_730+46delinsAAGAATAGACTTCC	NP_003989.2:n.730+33_730+46delinsAAGAATAGACTTCC
XM_011532006.1:c.751+33_751+46delinsAAGAATAGACTTCC	XP_011530308.1:n.751+33_751+46delinsAAGAATAGACTTCC
XM_011532007.1:c.727+33_727+46delinsAAGAATAGACTTCC	XP_011530309.1:n.727+33_727+46delinsAAGAATAGACTTCC
XM_011532008.1:c.572-1463_572-1450delinsAAGAATAGACTTCC	XP_011530310.1:n.572-1463_572-1450delinsAAGAATAGACTTCC
XM_011532009.1:c.334+33_334+46delinsAAGAATAGACTTCC	XP_011530311.1:n.334+33_334+46delinsAAGAATAGACTTCC
NM_001319226.1:c.727+33_727+46delinsAAGAATAGACTTCC	NP_001306155.1:n.727+33_727+46delinsAAGAATAGACTTCC
XM_011532006.2:c.751+33_751+46delinsAAGAATAGACTTCC	XP_011530308.1:n.751+33_751+46delinsAAGAATAGACTTCC
XM_024454067.1:c.754+33_754+46delinsAAGAATAGACTTCC	XP_024309835.1:n.754+33_754+46delinsAAGAATAGACTTCC
XM_024454068.1:c.730+33_730+46delinsAAGAATAGACTTCC	XP_024309836.1:n.730+33_730+46delinsAAGAATAGACTTCC
XM_024454069.1:c.596-1463_596-1450delinsAAGAATAGACTTCC	XP_024309837.1:n.596-1463_596-1450delinsAAGAATAGACTTCC
NM_003998.4:c.730+33_730+46delinsAAGAATAGACTTCC MANE Select	NP_003989.2:n.730+33_730+46delinsAAGAATAGACTTCC
NM_001165412.2:c.727+33_727+46delinsAAGAATAGACTTCC	NP_001158884.1:n.727+33_727+46delinsAAGAATAGACTTCC
NM_001319226.2:c.727+33_727+46delinsAAGAATAGACTTCC	NP_001306155.1:n.727+33_727+46delinsAAGAATAGACTTCC
NM_001382625.1:c.730+33_730+46delinsAAGAATAGACTTCC	NP_001369554.1:n.730+33_730+46delinsAAGAATAGACTTCC
NM_001382626.1:c.730+33_730+46delinsAAGAATAGACTTCC	NP_001369555.1:n.730+33_730+46delinsAAGAATAGACTTCC
NM_001382627.1:c.727+33_727+46delinsAAGAATAGACTTCC	NP_001369556.1:n.727+33_727+46delinsAAGAATAGACTTCC
NM_001382628.1:c.688+33_688+46delinsAAGAATAGACTTCC	NP_001369557.1:n.688+33_688+46delinsAAGAATAGACTTCC